Label: SANITIZER- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 70143-1001-1, 70143-1001-3 - Packager: Gandang Kalikasan USA 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 December 30, 2019
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- Official Label (Printer Friendly)
- Active Ingredient
- Uses:
- Purpose
- Warnings
- Directions
- DOSAGE & ADMINISTRATION
- Inactive Ingredients
- Principal display panel
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INGREDIENTS AND APPEARANCE
SANITIZER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70143-1001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 60 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70143-1001-1 50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/08/2015 2 NDC:70143-1001-3 200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 12/08/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/08/2015 Labeler - Gandang Kalikasan USA Inc. (024656271)