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blackberry vanilla hand sanitizer - 49035-107-02 - (Alcohol)

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Drug Information of blackberry vanilla hand sanitizer

Product NDC: 49035-107
Proprietary Name: blackberry vanilla hand sanitizer
Non Proprietary Name: Alcohol
Active Ingredient(s): 75    g/100mL & nbsp;   Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of blackberry vanilla hand sanitizer

Product NDC: 49035-107
Labeler Name: Wal-Mart Stores Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130521

Package Information of blackberry vanilla hand sanitizer

Package NDC: 49035-107-02
Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE (49035-107-02) > 30 mL in 1 BOTTLE, PLASTIC (49035-107-01)

NDC Information of blackberry vanilla hand sanitizer

NDC Code 49035-107-02
Proprietary Name blackberry vanilla hand sanitizer
Package Description 1 BOTTLE, PLASTIC in 1 PACKAGE (49035-107-02) > 30 mL in 1 BOTTLE, PLASTIC (49035-107-01)
Product NDC 49035-107
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Alcohol
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20130521
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Wal-Mart Stores Inc
Substance Name ALCOHOL
Strength Number 75
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of blackberry vanilla hand sanitizer


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