Label: HAND SANITIZER- alcohol, water gel
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Contains inactivated NDC Code(s)
NDC Code(s): 78837-202-20 - Packager: Phoenix Wipes Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 8, 2020
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol, water gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78837-202 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 70 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 1-(3,4-DIMETHOXYPHENYL)PROPANE-1,2-DIOL (UNII: N6222F124L) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78837-202-20 1 mL in 1 PACKET; Type 0: Not a Combination Product 06/12/2020 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/12/2020 Labeler - Phoenix Wipes Inc (117544823)
70 % Alcohol vv Purpose: Antiseptic
2ml NDC 78837-202-20