BEAUTAIME HAND DOCTOR- alcohol gel

BEAUTAIME HAND DOCTOR by

Drug Labeling and Warnings

BEAUTAIME HAND DOCTOR by is a Otc medication manufactured, distributed, or labeled by ASAN C&S. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: ETHANOL 62.0% w/w

INACTIVE INGREDIENT

Inactive ingredients

Water, Glycerin, Propylene Glycol, Triethanolamine, Carbomer, Aloe Barbadensis Leaf Powder, Aloe Extract

PURPOSE

Purpose: ANTISEPTIC

WARNINGS

Warnings

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

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

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

PACKAGE LABEL - BEAUTAIME HAND DOCTOR GEL 70mL

PACKAGE LABEL - BEAUTAIME HAND DOCTOR GEL 500mL

INGREDIENTS AND APPEARANCE

BEAUTAIME HAND DOCTOR 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73697-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Propylene Glycol (UNII: 6DC9Q167V3)
Trolamine (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73697-110-01	70 mL in 1 CONTAINER; Type 0: Not a Combination Product	04/01/2020
2	NDC: 73697-110-02	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/01/2020

Labeler - ASAN C&S (631139649)

Registrant - ASAN C&S (631139649)

Establishment
Name	Address	ID/FEI	Business Operations
ASAN C&S		631139649	manufacture(73697-110)