HAND SANITIZER- alcohol gel 
Zink Holdings LLC

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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Zink Brntag Crayola Blue Sanitizer Gel Alc75

Active Ingredient

Alcohol 75%v/v

Purpose

Antiseptic

Uses

■ Hand Sanitizer to help reduce bacteria on the skin. 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, ears and mouth. In case of eye contact immediately flush eyes thoroughly with water

Stop use and ask a doctor

if irritation or rash occurs. These may be the signs of a serious condition.

Keep out of reach of children

In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.

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 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Inactive ingredients

FD&C Blue 1, Glycerin, Hydroxypropyl Cellulose, Water

Inner Package Label

inner package label

Outer Package Label

outer package label

Outer Package Label

outer package label

Package Label

package label

Package Label

package label

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79332-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
WATER (UNII: 059QF0KO0R)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79332-003-088 in 1 BOX08/21/2020
1NDC:79332-003-0160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:79332-003-044 in 1 BOX08/21/2020
2NDC:79332-003-0160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:79332-003-021 in 1 BOX08/21/2020
3NDC:79332-003-0160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:79332-003-80236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/10/2020
5NDC:79332-003-16499 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/21/2020
Labeler - Zink Holdings LLC (117561710)

Revised: 9/2020
Document Id: af7489bc-d1f4-e067-e053-2a95a90aedb2
Set id: ad6a1fdd-1b93-6a64-e053-2995a90a2d40
Version: 2
Effective Time: 20200916
 
Zink Holdings LLC