Label: 70% ETHANOL 16OZ. liquid
- NDC Code(s): 79071-1003-0
- Packager: Riviera Beverages, LLC
- 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.
Updated February 9, 2021
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SPL UNCLASSIFIED SECTION
This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.
The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:
- Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
- Glycerol (1.45% v/v).
- Hydrogen peroxide (0.125% v/v).
- Sterile distilled water or boiled cold water.
The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.
- Active Ingredient(s)
- Do not use
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- 70% Ethanol Sanitzer
INGREDIENTS AND APPEARANCE
70% ETHANOL 16OZ.
70% ethanol 16oz. liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79071-1003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 350 mL in 500 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) 0.5 mL in 500 mL FRAGRANCE EUCALYPTUS SPEARMINT ORC1601627 (UNII: E90O5M6HMB) 0.7 mL in 500 mL GLYCERIN (UNII: PDC6A3C0OX) 1 mL in 500 mL .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) 0.1 mL in 500 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.01 mL in 500 mL Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79071-1003-0 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 02/01/2021 Labeler - Riviera Beverages, LLC (021785705) Registrant - Riviera Beverages, LLC (021785705) Establishment Name Address ID/FEI Business Operations Riviera Beverages, LLC. 021785705 manufacture(79071-1003)