Label: ALL-PURPOSE SANITIZER- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 77110-108-02, 77110-108-03 - Packager: Biominerales Pharma
- 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 August 11, 2020
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive Ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 499.79 ML Bottle Label
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INGREDIENTS AND APPEARANCE
ALL-PURPOSE SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77110-108 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 GLYCERIN (UNII: PDC6A3C0OX) HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77110-108-03 499.79 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/12/2020 2 NDC:77110-108-02 946.35 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 08/12/2020 Labeler - Biominerales Pharma (117489663) Establishment Name Address ID/FEI Business Operations Biominerales Pharma 117489663 MANUFACTURE(77110-108)