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6505-00-116-1740

20 Products

PHIS0HEX

DETERGENT,SURGICAL

NSN, MFG P/N

6505001161740

NSN

6505-00-116-1740

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PHIS0HEX

DETERGENT,SURGICAL

NSN, MFG P/N

6505001161740

NSN

6505-00-116-1740

MFG

STERLING-WINTHROP RESEARCH INSTITUTE A DIV OF STERLING DRUG INC

Description

INGREDIENT CLASSIFICATION: MEDICATED
MANUFACTURERS CODE: 81348
NON-DEFINITIVE GOVERNMENT SPEC/STD REFERENCE: PD240
NONDEFINITIVE SPEC/STD DATA: 1 SIZE
SPEC/STD CONTROLLING DATA:
STRENGTH: 50.000 PERCENT DETERGENT AGENT BLANK AND 8.000 PERCENT EMOLLIENTS BLANK AND 3.000 PERCENT HEXACHLOROPHENE BLANK AND 39.000 PERCENT LIQUIDS BLANK

2B2304

RINGER'S INJECTION,USP

NSN, MFG P/N

6505001161091

NSN

6505-00-116-1091

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2B2304

RINGER'S INJECTION,USP

NSN, MFG P/N

6505001161091

NSN

6505-00-116-1091

MFG

BAXTER HEALTHCARE CORP IV SYSTEMS/GOV SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.330 MILLIGRAMS CALCIUM CHLORIDE PER MILLILITER AND 0.300 MILLIGRAMS PUCHERITE PER MILLILITER AND 8.600 MILLIGRAMS SODIUM CHLORIDE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: RINGERS INJECTION USP 1000 ML 14S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: W/OVERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 14

NDC00338-0105-04

RINGER'S INJECTION,USP

NSN, MFG P/N

6505001161091

NSN

6505-00-116-1091

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NDC00338-0105-04

RINGER'S INJECTION,USP

NSN, MFG P/N

6505001161091

NSN

6505-00-116-1091

MFG

BAXTER HEALTHCARE CORP IV SYSTEMS/GOV SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.330 MILLIGRAMS CALCIUM CHLORIDE PER MILLILITER AND 0.300 MILLIGRAMS PUCHERITE PER MILLILITER AND 8.600 MILLIGRAMS SODIUM CHLORIDE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: RINGERS INJECTION USP 1000 ML 14S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: W/OVERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 14

2B1323

SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505001161120

NSN

6505-00-116-1120

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2B1323

SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505001161120

NSN

6505-00-116-1120

MFG

BAXTER HEALTHCARE CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.900 PERCENTAGE, W/V SODIUM CHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: W/OVERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 12

2B1803

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161134

NSN

6505-00-116-1134

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2B1803

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161134

NSN

6505-00-116-1134

MFG

BAXTER HEALTHCARE CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 18.700 MILLIGRAMS SODIUM LACTATE PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM LACTATE INJECTION USP 500 ML BAG 12 BAGS PER BOX
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: EA MOLAR SOLUTION CONTAINS 1.0 GRAM-MOECULAR WEIGHT OF THE ACTIVE INGREDIENT IN EACH LITER OF SOLUTION
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: 1/6 MOLAR; W/O VERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 12

NDC00338-0129-03

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161134

NSN

6505-00-116-1134

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NDC00338-0129-03

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161134

NSN

6505-00-116-1134

MFG

BAXTER HEALTHCARE CORP IV SYSTEMS/GOV SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 18.700 MILLIGRAMS SODIUM LACTATE PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM LACTATE INJECTION USP 500 ML BAG 12 BAGS PER BOX
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: EA MOLAR SOLUTION CONTAINS 1.0 GRAM-MOECULAR WEIGHT OF THE ACTIVE INGREDIENT IN EACH LITER OF SOLUTION
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: 1/6 MOLAR; W/O VERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 12

2B1804

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161158

NSN

6505-00-116-1158

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2B1804

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161158

NSN

6505-00-116-1158

MFG

BAXTER HEALTHCARE CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 18.700 MILLIGRAMS SODIUM LACTATE PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM LACTATE INJECTION USP 1000 ML BAG 12 BAGS PER PACKAGE
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: ENMOLAR SOLUTION CONTAINS 1.0 GRAM-MOLECULAR WEIGHT OF THE ACTIVE INGREDIENT IN EACH LITER OF SOLUTION
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: 1/6 MOLAR; W/OVERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 12

NDC00338-0129-04

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161158

NSN

6505-00-116-1158

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NDC00338-0129-04

SODIUM LACTATE INJECTION,USP

NSN, MFG P/N

6505001161158

NSN

6505-00-116-1158

MFG

BAXTER HEALTHCARE CORP IV SYSTEMS/GOV SALES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 18.700 MILLIGRAMS SODIUM LACTATE PER MILLILITER
ADMINISTRATION: INTRAVENOUS
FEATURES PROVIDED: STERILE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM LACTATE INJECTION USP 1000 ML BAG 12 BAGS PER PACKAGE
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
III SUPPLEMENTARY FEATURES: ENMOLAR SOLUTION CONTAINS 1.0 GRAM-MOLECULAR WEIGHT OF THE ACTIVE INGREDIENT IN EACH LITER OF SOLUTION
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 MILLILITERS
PRIMARY CONTAINER TYPE: BAG, PLASTIC
SPECIAL FEATURES: 1/6 MOLAR; W/OVERPOUCH AS WATER VAPOR BARRIER
TOTAL PRIMARY CONTAINER QUANTITY: 12

F0STEXCREAM

SULFUR AND SALICYLIC ACID OINTMENT

NSN, MFG P/N

6505001161316

NSN

6505-00-116-1316

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F0STEXCREAM

SULFUR AND SALICYLIC ACID OINTMENT

NSN, MFG P/N

6505001161316

NSN

6505-00-116-1316

MFG

BRISTOL-MYERS SQUIBB CO WESTWOOD-SQUIBB PHARMACEUTICALS DIV

Description

ACTIVE INGREDIENT AND STRENGTH: 2.000 SALICYLIC ACID PERCENTAGE, W/W AND 2.000 SULFUR PERCENTAGE, W/W
ADMINISTRATION: TOPICAL
PRIMARY CONTAINER CONTENT QUANTITY: 4.500 OUNCES
PRIMARY CONTAINER TYPE: JAR

NDC00536-1962-97

SULFUR AND SALICYLIC ACID SHAMPOO

NSN, MFG P/N

6505001161362

NSN

6505-00-116-1362

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NDC00536-1962-97

SULFUR AND SALICYLIC ACID SHAMPOO

NSN, MFG P/N

6505001161362

NSN

6505-00-116-1362

MFG

WATSON PHARMA INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.000 PERCENTAGE, W/V SULFUR ACTIVE INGREDIENT AND 2.000 PERCENTAGE, W/V SALICYLIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SULFUR AND SALICYLIC ACID SHAMPOO 4 OZ BOTTLE
PRIMARY CONTAINER CONTENT QUANTITY: 4.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: PH RANGE OF 3.2 TO 4.0; SURFACE ACTIVE,PENETRATING,THERAPEUTIC,ANTI SEBORRHEIC SHAMPOO IN A COLORED,SCENTED,SURFACE ACTIVE SHAMPOO BASE

METHERGINE

METHYLERGONOVINE MALEATE INJECTION,USP

NSN, MFG P/N

6505001161374

NSN

6505-00-116-1374

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METHERGINE

METHYLERGONOVINE MALEATE INJECTION,USP

NSN, MFG P/N

6505001161374

NSN

6505-00-116-1374

MFG

NOVARTIS PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.200 MILLIGRAMS METHYLERGONOVINE MALEATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLERGONOVINE MALEATE INJECTION USP 0.2 MG CC 1 ML AMPUL 20 BOX
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 MILLILITERS
PRIMARY CONTAINER TYPE: AMPUL
TOTAL PRIMARY CONTAINER QUANTITY: 20

NDC00078-0053-03

METHYLERGONOVINE MALEATE INJECTION,USP

NSN, MFG P/N

6505001161374

NSN

6505-00-116-1374

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NDC00078-0053-03

METHYLERGONOVINE MALEATE INJECTION,USP

NSN, MFG P/N

6505001161374

NSN

6505-00-116-1374

MFG

AMERISOURCEBERGEN DRUG CORPORATION DIV CORPORATE OFFICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.200 MILLIGRAMS METHYLERGONOVINE MALEATE PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: METHYLERGONOVINE MALEATE INJECTION USP 0.2 MG CC 1 ML AMPUL 20 BOX
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 1.000 MILLILITERS
PRIMARY CONTAINER TYPE: AMPUL
TOTAL PRIMARY CONTAINER QUANTITY: 20

NDC00054-3716-63

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

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NDC00054-3716-63

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

MFG

BOEHRINGER INGELHEIM ROXANE INC. DIV SUB OF BOEHRINGER INGELHEIM CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V POTASSIUM CHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM CHLORIDE ORAL SOLUTION USP 10% SUGAR-FREE 16 FL OZ
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SUGAR-FREE

NDC00182-6120-40

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

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NDC00182-6120-40

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V POTASSIUM CHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM CHLORIDE ORAL SOLUTION USP 10% SUGAR-FREE 16 FL OZ
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SUGAR-FREE

NDC00536-1700-85

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

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NDC00536-1700-85

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

MFG

RUGBY GROUP INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V POTASSIUM CHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM CHLORIDE ORAL SOLUTION USP 10% SUGAR-FREE 16 FL OZ
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SUGAR-FREE

NDC00904-1007-16

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

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NDC00904-1007-16

POTASSIUM CHLORIDE ORAL SOLUTION,USP

NSN, MFG P/N

6505001161459

NSN

6505-00-116-1459

MFG

MAJOR PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 10.000 PERCENTAGE, W/V POTASSIUM CHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POTASSIUM CHLORIDE ORAL SOLUTION USP 10% SUGAR-FREE 16 FL OZ
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PRIMARY CONTAINER CONTENT QUANTITY: 16.000 FLUID OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: SUGAR-FREE

DECHOLIN

DEHYDROCHOLIC ACID TABLETS,USP

NSN, MFG P/N

6505001161635

NSN

6505-00-116-1635

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DECHOLIN

DEHYDROCHOLIC ACID TABLETS,USP

NSN, MFG P/N

6505001161635

NSN

6505-00-116-1635

MFG

BAYER PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS DEHYDROCHOLIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEHYDROCHOLIC ACID TABLETS USP 250 MG 100 TABLETS PER BOTTLE
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

DECHOLIN TABLETS

DEHYDROCHOLIC ACID TABLETS,USP

NSN, MFG P/N

6505001161635

NSN

6505-00-116-1635

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DECHOLIN TABLETS

DEHYDROCHOLIC ACID TABLETS,USP

NSN, MFG P/N

6505001161635

NSN

6505-00-116-1635

MFG

BAYER PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS DEHYDROCHOLIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEHYDROCHOLIC ACID TABLETS USP 250 MG 100 TABLETS PER BOTTLE
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00026-8121-51

DEHYDROCHOLIC ACID TABLETS,USP

NSN, MFG P/N

6505001161635

NSN

6505-00-116-1635

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NDC00026-8121-51

DEHYDROCHOLIC ACID TABLETS,USP

NSN, MFG P/N

6505001161635

NSN

6505-00-116-1635

MFG

BAYER PHARMACEUTICALS CORPORATION

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 250.000 MILLIGRAMS DEHYDROCHOLIC ACID ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DEHYDROCHOLIC ACID TABLETS USP 250 MG 100 TABLETS PER BOTTLE
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

PD240

DETERGENT,SURGICAL

NSN, MFG P/N

6505001161740

NSN

6505-00-116-1740

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PD240

DETERGENT,SURGICAL

NSN, MFG P/N

6505001161740

NSN

6505-00-116-1740

MFG

FEDERAL SPECIFICATIONS PROMULGATED BY GENERAL SERVICES ADMINISTRATION WASHINGTON DC

Description

INGREDIENT CLASSIFICATION: MEDICATED
MANUFACTURERS CODE: 81348
NON-DEFINITIVE GOVERNMENT SPEC/STD REFERENCE: PD240
NONDEFINITIVE SPEC/STD DATA: 1 SIZE
SPEC/STD CONTROLLING DATA:
STRENGTH: 50.000 PERCENT DETERGENT AGENT BLANK AND 8.000 PERCENT EMOLLIENTS BLANK AND 3.000 PERCENT HEXACHLOROPHENE BLANK AND 39.000 PERCENT LIQUIDS BLANK