Label: NORDIC WELLNESS VITAMIN C HAND SANITIZER- ethyl alcohol formulation liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 79655-804-01 - Packager: Kala Corporation
- Category: HUMAN OTC DRUG LABEL
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 13, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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
- Nordic Wellness™ Vitamin C Hand Sanitizer
-
INGREDIENTS AND APPEARANCE
NORDIC WELLNESS VITAMIN C HAND SANITIZER
ethyl alcohol formulation liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79655-804 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 38.35 mL in 59 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 18.88 mL in 59 mL ORANGE (UNII: 5EVU04N5QU) 0.06 mL in 59 mL LINALYL ACETATE (UNII: 5K47SSQ51G) 0.04 mL in 59 mL DECANAL (UNII: 31Z90Q7KQJ) 0.01 mL in 59 mL .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF) 0.03 mL in 59 mL LINALOOL, (+/-)- (UNII: D81QY6I88E) 0.01 mL in 59 mL CITRONELLYL NITRILE, (+/-)- (UNII: GP9AT16H16) 0.01 mL in 59 mL CAPRYLALDEHYDE (UNII: XGE9999H19) 0.01 mL in 59 mL NERAL (UNII: 8M466BQL1X) 0.01 mL in 59 mL ETHYL ANTHRANILATE (UNII: 38Y050IUE4) 0.01 mL in 59 mL 2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS) 0.01 mL in 59 mL GLYCERIN (UNII: PDC6A3C0OX) 0.885 mL in 59 mL ALLYL HEXANOATE (UNII: 3VH84A363D) 0.01 mL in 59 mL ETHYL MALTOL (UNII: L6Q8K29L05) 0.01 mL in 59 mL .DELTA.-DAMASCONE (UNII: 7F4RIE5P7E) 0.01 mL in 59 mL CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) 0.06 mL in 59 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79655-804-01 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/18/2020 Labeler - Kala Corporation (623014826) Registrant - Kala Corporation (623014826) Establishment Name Address ID/FEI Business Operations Kala Corporation 623014826 manufacture(79655-804)