Blinc Antibacterial Sanitizer Moisturizing Gel

Blinc Antibacterial Sanitizer Moisturizing by

Drug Labeling and Warnings

Blinc Antibacterial Sanitizer Moisturizing by is a Otc medication manufactured, distributed, or labeled by BLINC INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BLINC ANTIBACTERIAL SANITIZER MOISTURIZING- alcohol gel 
BLINC 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.

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Blinc Antibacterial Sanitizer Moisturizing Gel

DRUG FACTS

Active ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

USE

Hand sanitizer to help reduce bacteria on the skin.

WARNINGS

Flammable. Keep away from fire or flame.

For external use only.

When using this product 

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor

if irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• Put enough product in your palm to cover hands and rub hands together until dry.
• Children under 6 years of age should be supervised when using this product.

OTHER INFORMATION

• Store below 110°F (43°C).
• May discolor certain fabric surfaces.

INACTIVE INGREDIENTS

Water/Aqua, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice.

Package Labeling

Package Labeling:147ml

BLINC ANTIBACTERIAL SANITIZER MOISTURIZING 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78932-005
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
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78932-005-31	925 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2020	12/31/2022
2	NDC: 78932-005-05	147 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/31/2020	12/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/31/2020	12/31/2022

Labeler - BLINC INC (071689652)

Revised: 10/2022

Document Id: eb503c50-fada-b68a-e053-2995a90a5796

34390-5

Set id: a82afc26-c948-67c8-e053-2a95a90aa5df

Version: 3

Effective Time: 20221018