Label: PHARMACYS PRESCRIPTION 2PK 2OZ HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72197-002-02 - Packager: American Consumer Products Corp
- 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 December 31, 2019
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- Active Ingredient
- Purpose
- Warnings
- Stop Use
- Keep out of reach of children
- Inactive Ingredients
- Indications & Usage Section
- Other Information
- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PHARMACYS PRESCRIPTION 2PK 2OZ HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72197-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL 2-(2-METHYLBUTYRATE) (UNII: 3Z73C506A9) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) GLYCERIN (UNII: PDC6A3C0OX) TRIETHANOLAMINE 2-CYCLOHEXYL-4,6-DINITROPHENOLATE (UNII: N2TK31JIAH) ALOE ARBORESCENS WHOLE (UNII: 0EF00WD7LU) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72197-002-02 59.14 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/28/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/28/2018 Labeler - American Consumer Products Corp (081101181)