Label: PHARMACYS PRESCRIPTION HAND SANITIZER- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 72197-023-05 - 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 April 28, 2020
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- Active Ingredient
- Purpose
- Warnings
- Indications & Usage Section
- Stop Use
- Keep out of reach of children
- Directions
- Other Information
- Inactive Ingredients
- Distributed By
- Pharmacys Prescription Hand Sanitizer
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INGREDIENTS AND APPEARANCE
PHARMACYS PRESCRIPTION HAND SANITIZER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72197-023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72197-023-05 147 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/16/2020 Labeler - American Consumer Products Corp (081101181)