Hand Sanitizer 70%, Alcohol Antiseptic Gel

Hand Sanitizer 70 Alcohol Antiseptic by

Drug Labeling and Warnings

Hand Sanitizer 70 Alcohol Antiseptic by is a Otc medication manufactured, distributed, or labeled by Hyatt Life Sciences, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER 70 ALCOHOL ANTISEPTIC- alcohol gel 
Hyatt Life Sciences, Inc.

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.

----------

Hand Sanitizer 70%, Alcohol Antiseptic Gel

Drug Facts

Active ingredient[s]

Alcohol 70% v/v

Purpose

Antiseptic

Use[s]

Hand sanitizer 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 two 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 on hands to cover all surfaces. Rub hands 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

Water, Glycerin, Carbomer 940, Triethanolamine, Hydrogen Peroxide

Package Labeling:

Label

Package Labeling: 72933-003-02

Label2

Package Labeling: 72933-003-03

Label3

Package Labeling: 72933-003-04

Label4

Package Labeling:

Bottle

Package Labeling:

Bottle0

HAND SANITIZER 70 ALCOHOL ANTISEPTIC 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 72933-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
TROLAMINE (UNII: 9O3K93S3TK)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 72933-003-01473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/14/202003/31/2022
2NDC: 72933-003-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product07/23/202003/31/2022
3NDC: 72933-003-03296 mL in 1 BOTTLE; Type 0: Not a Combination Product07/23/202003/31/2022
4NDC: 72933-003-043785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/23/202003/31/2022
5NDC: 72933-003-0518927 mL in 1 PAIL; Type 0: Not a Combination Product07/29/202003/31/2022
6NDC: 72933-003-061182 mL in 1 BOTTLE; Type 0: Not a Combination Product07/29/202003/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/14/202003/31/2022
Labeler - Hyatt Life Sciences, Inc. (117495900)

Revised: 9/2022
Document Id: e9bdedee-93df-1e19-e053-2a95a90a6377
Set id: a9fe2951-bb6a-4d16-aad1-ca62ca413c5e
Version: 5
Effective Time: 20220928