DR.BETTER HOMES HAND SANITIZER- alcohol gel 
UI COSMETICS CO., 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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Active Ingredient

Ethanol 70%

Purpose

Antiseptic

Uses

To help reduce bacteria on the skin

Warnings

For external use only.

Flammable, keep away from heat or flames.

When using this product

keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask doctor if

irritation and redness develop and persist.

Keep out of reach of children.

Directions

Apply a small amount in your palm and rub hands together briskly until dry.

Supervise children under 6 years in the use of product.

Other Information

Protect this product from excessive heat and direct sun.

Inactive Ingredients

Glycerin, Sodium Hyaluronate, Carbomer, Butylene Glycol, Aloe Extract, Triethanolamine, Flavoring, Purified Water

Package Label

75615-0020-0 10000ml

75615-0020-1 500ml

75615-0020-2 50ml

75615-0020-3 60ml

75615-0020-4 100ml

75615-0020-5 200ml

75615-0020-6 250ml

75615-0020-7 300ml

75615-0020-8 5000ml

75615-0020-9 3785ml

DR.BETTER HOMES HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75615-0020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)  
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ALOE (UNII: V5VD430YW9)  
TROLAMINE (UNII: 9O3K93S3TK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75615-0020-1500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/08/2020
2NDC:75615-0020-250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/21/2020
3NDC:75615-0020-360 mL in 1 BOTTLE; Type 0: Not a Combination Product05/21/2020
4NDC:75615-0020-4100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/21/2020
5NDC:75615-0020-5200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2020
6NDC:75615-0020-6250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2020
7NDC:75615-0020-7300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2020
8NDC:75615-0020-85000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/26/2020
9NDC:75615-0020-93785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/22/2020
10NDC:75615-0020-010000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/22/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/08/2020
Labeler - UI COSMETICS CO., LTD (688362189)
Registrant - UI COSMETICS CO., LTD (688362189)
Establishment
NameAddressID/FEIBusiness Operations
UI COSMETICS CO., LTD688362189manufacture(75615-0020)

Revised: 1/2021
Document Id: b9660dcf-6888-a1cb-e053-2995a90a3199
Set id: a50602e4-2d20-1d8c-e053-2a95a90aff28
Version: 5
Effective Time: 20210121
 
UI COSMETICS CO., LTD