Label: ADVANCED HAND SANITIZER- ethyl alcohol gel
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NDC Code(s):
83986-439-16,
83986-439-32,
83986-439-34,
83986-439-50, view more83986-439-86
- Packager: UpLift Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 23, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Disclaimer
- Advrse Reaction
- Principal display panel
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INGREDIENTS AND APPEARANCE
ADVANCED HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83986-439 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 WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N) GLYCERIN (UNII: PDC6A3C0OX) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) SULISOBENZONE (UNII: 1W6L629B4K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83986-439-16 59 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 02/23/2024 2 NDC:83986-439-34 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/23/2024 3 NDC:83986-439-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/23/2024 4 NDC:83986-439-32 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/23/2024 5 NDC:83986-439-50 709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/23/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 02/23/2024 Labeler - UpLift Brands LLC (119091527) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(83986-439) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(83986-439)