BEAUTAIME HAND DOCTOR- alcohol gel 
ASAN C&S

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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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

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PACKAGE LABEL - BEAUTAIME HAND DOCTOR GEL 500mL

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BEAUTAIME HAND DOCTOR 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73697-110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73697-110-0170 mL in 1 CONTAINER; Type 0: Not a Combination Product04/01/2020
2NDC:73697-110-02500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/01/2020
Labeler - ASAN C&S (631139649)
Registrant - ASAN C&S (631139649)
Establishment
NameAddressID/FEIBusiness Operations
ASAN C&S631139649manufacture(73697-110)

Revised: 4/2020
Document Id: ca28ef98-a013-48a5-a6a7-0c750685b5fa
Set id: fc2d2b4f-3293-42a9-8e1b-acacba300717
Version: 1
Effective Time: 20200418
 
ASAN C&S