Label: DR.BETTER HOMES HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75615-0020-0, 75615-0020-1, 75615-0020-2, 75615-0020-3, view more75615-0020-4, 75615-0020-5, 75615-0020-6, 75615-0020-7, 75615-0020-8, 75615-0020-9 - Packager: UI COSMETICS CO., LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated January 21, 2021
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask doctor if
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
DR.BETTER HOMES HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75615-0020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:75615-0020-1 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/08/2020 2 NDC:75615-0020-2 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2020 3 NDC:75615-0020-3 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2020 4 NDC:75615-0020-4 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2020 5 NDC:75615-0020-5 200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/21/2020 6 NDC:75615-0020-6 250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/21/2020 7 NDC:75615-0020-7 300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/21/2020 8 NDC:75615-0020-8 5000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/26/2020 9 NDC:75615-0020-9 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/22/2020 10 NDC:75615-0020-0 10000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/08/2020 Labeler - UI COSMETICS CO., LTD (688362189) Registrant - UI COSMETICS CO., LTD (688362189) Establishment Name Address ID/FEI Business Operations UI COSMETICS CO., LTD 688362189 manufacture(75615-0020)