Cinital Hand Sanitizer by Shenzhen Tianheyuan Enterprise Ltd. Cinital Hand Sanitizer

Cinital Hand Sanitizer by

Drug Labeling and Warnings

Cinital Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shenzhen Tianheyuan Enterprise Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CINITAL HAND SANITIZER- alcohol gel 
Shenzhen Tianheyuan Enterprise Ltd.

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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Cinital Hand Sanitizer

Drug Facts

Active Ingredients

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses:

Hand Sanitizer to help reduce bacteria on skin

Warnings:

For external use only.

Flammable. Keep away from heat or flame.

When using this product

• Avoid contact with eyes. In case of contact rinse with water.
• Do not inhale or ingest.
• Avoid contact with broken skin.

Stop use and ask a doctor 

if skin irritation develops.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

• Wet hands thoroughly and rub together until dry.
• Audlt supervision for children under 6.
• Not for infants.

Other information

• Store between 15°-30°C (59°-86°F).
• May discolor fabrics

Inactive Ingredients:

Water (Aqua), Butylene Glycol, Acrylates/C10-30 Alkyl Arylate Crosspolymer, Aloe Barbadensis Leaf Juice, Triethanolamine, Citric Acid.

Package Labeling:

CINITAL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70187-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70187-001-01	29 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/03/2020	06/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/03/2020	06/03/2020

Labeler - Shenzhen Tianheyuan Enterprise Ltd. (529112662)

Revised: 9/2022

Document Id: e9ab8bad-1a08-0555-e053-2995a90a2cdd

34390-5

Set id: 53b55cef-98dc-4033-953a-de107f68425d

Version: 2

Effective Time: 20220927