BUFFERIN® HAND SANITIZER

Bufferin Hand Sanitizer by

Drug Labeling and Warnings

Bufferin Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Genomma Lab USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BUFFERIN HAND SANITIZER- alcohol gel 
Genomma Lab USA

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.

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BUFFERIN® HAND SANITIZER

Drug Facts

Active Ingredient

Ethyl alcohol 70% v/v

Purpose

Antiseptic

Uses

• To decrease bacteria on the skin when water, soap & towel are not available
• Recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

When using this product

• Avoid contact with eyes. In case of contact with eyes, rinse thoroughly with water.
• Do not use on broken or irritated skin.

Stop use and ask a doctor if if skin irritation or redness occurs and last more than 3 days.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply enough product to wet hands. Rub hands together until dry. Supervise children in use of this product.

Other information

• Do not store above 105 °F (40 °C).
• May discolor certain fabrics and wood surfaces.

Inactive ingredients

Water, propylene glycol, glycerin, aloe barbadensis extract, tocopheryl acetate, fragrance, PEG-6, Acrylates/Vinyl Isodecanoate Crosspolymer

Questions?

Call toll free 1-877-994-3666
Monday to Friday, 8am to 6pm, Central time

Distributed by: Genomma Lab USA
Inc., Houston, TX, 77027
www.genommalab.us

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

The Science
of Healthy Hands

70% ETHYL ALCOHOL
SOURCED IN THE USA

BUFFERIN
HAND SANITIZER

Antibacterial Gel

KILLS 99.99%
OF BACTERIA

enriched with
Vitamin E & Aloe

8 fl oz
(236 ml)

BUFFERIN HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50066-609
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Glycerin (UNII: PDC6A3C0OX)
Water (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
Propylene glycol (UNII: 6DC9Q167V3)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50066-609-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/11/2020	11/11/2022
2	NDC: 50066-609-02	70 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/03/2021	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/11/2020	11/11/2022

Labeler - Genomma Lab USA (832323534)

Revised: 7/2022

Document Id: 87918f3c-2a49-4d21-802f-287f8216eecb

34390-5

Set id: 37060747-b875-4417-a895-4838176612be

Version: 3

Effective Time: 20220718