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PURE SPRING - 11822-4670-9 - (ETHYL ALCOHOL)

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Drug Information of PURE SPRING

Product NDC: 11822-4670
Proprietary Name: PURE SPRING
Non Proprietary Name: ETHYL ALCOHOL
Active Ingredient(s): 62    mL/100mL & nbsp;   ETHYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of PURE SPRING

Product NDC: 11822-4670
Labeler Name: RITE AID CORPORATION
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120319

Package Information of PURE SPRING

Package NDC: 11822-4670-9
Package Description: 260 mL in 1 BOTTLE, PLASTIC (11822-4670-9)

NDC Information of PURE SPRING

NDC Code 11822-4670-9
Proprietary Name PURE SPRING
Package Description 260 mL in 1 BOTTLE, PLASTIC (11822-4670-9)
Product NDC 11822-4670
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ETHYL ALCOHOL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120319
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name RITE AID CORPORATION
Substance Name ALCOHOL
Strength Number 62
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of PURE SPRING


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