Label: 75% ALCOHOL INSTANT HAND SANITIZER gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75879-001-01, 75879-001-02, 75879-001-03, 75879-001-04, view more75879-001-05, 75879-001-06, 75879-001-07, 75879-001-08, 75879-001-09, 75879-001-10, 75879-001-11, 75879-001-12, 75879-001-13, 75879-001-14, 75879-001-15, 75879-001-16 - Packager: FEEL LIFE CO.,LIMITED
- 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 May 11, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- DO NOT USE
- When using this product
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
75% ALCOHOL INSTANT HAND SANITIZER
75% alcohol instant hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75879-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75879-001-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 2 NDC:75879-001-02 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 3 NDC:75879-001-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 4 NDC:75879-001-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 5 NDC:75879-001-05 119 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 6 NDC:75879-001-06 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 7 NDC:75879-001-07 149 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 8 NDC:75879-001-08 199 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 9 NDC:75879-001-09 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 10 NDC:75879-001-10 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 11 NDC:75879-001-11 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 12 NDC:75879-001-12 349 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 13 NDC:75879-001-13 350 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 14 NDC:75879-001-14 499 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 15 NDC:75879-001-15 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 16 NDC:75879-001-16 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/11/2020 Labeler - FEEL LIFE CO.,LIMITED (421264782) Registrant - FEEL LIFE CO.,LIMITED (421264782) Establishment Name Address ID/FEI Business Operations FEEL LIFE CO.,LIMITED 421264782 manufacture(75879-001)
