Strike Bac Instant Hand Sanitizer

Strike Bac Instant Hand Sanitizer by

Drug Labeling and Warnings

Strike Bac Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Genlabs Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

STRIKE BAC INSTANT HAND SANITIZER- alcohol liquid 
Genlabs Corporation

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.

----------

Strike Bac Instant Hand Sanitizer

Drug Facts

Active ingredient[s]

Alcohol 70% v/v

Purpose

Antiseptic

Use[s]

Hand Sanitizer Gel to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

on children less than 2 months of age
on open skin wounds

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.

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15-30C (59-86F)
Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

aloe vera, fragrance, glycerin, polyacrylic acid polymer, purified water USP

Package Labeling:3.78L

Package Labeling:.946L

STRIKE BAC INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62569-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62569-002-01	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/02/2020	12/21/2021
2	NDC: 62569-002-02	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/02/2020	12/21/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/02/2020	12/21/2021

Labeler - Genlabs Corporation (064594260)

Revised: 1/2023

Document Id: f16feda1-b732-d2c4-e053-2995a90ae511

34390-5

Set id: a214e174-ff7d-4a2b-b668-852b6e2a829c

Version: 2

Effective Time: 20230104