Label: HAND SANITIZER MIST- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 71080-0023-1, 71080-0023-2, 71080-0023-3, 71080-0023-4, view more71080-0023-5 - Packager: GTG WELLNESS CO., LTD.
- 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 May 14, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
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WARNINGS
• Flammable. Keep away from heat and flame.
• For external use only.
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Do not use
• on children less than 2 months old, or on open skin wounds.--------------------------------------------------------------------------------------------------------
When using this product • avoid contact with eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor • if irritation or rash occurs. These may be signs of a serious condition. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Other information
- Questions
- 71080-0023-1: Hand Sanitizer Mist (Heat)
- 71080-0023-2: Hand Sanitizer Mist (Knicks)
- 71080-0023-3: Hand Sanitizer Mist (Lakers)
- 71080-0023-4: Hand Sanitizer Mist (Nets)
- 71080-0023-5: Hand Sanitizer Mist (NBA)
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INGREDIENTS AND APPEARANCE
HAND SANITIZER MIST
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) Alcohol 11.9 g in 17 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GRAPEFRUIT (UNII: O82C39RR8C) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71080-0023-1 17 mL in 1 CARTON; Type 0: Not a Combination Product 05/10/2021 2 NDC:71080-0023-2 17 mL in 1 CARTON; Type 0: Not a Combination Product 05/10/2021 3 NDC:71080-0023-3 17 mL in 1 CARTON; Type 0: Not a Combination Product 05/10/2021 4 NDC:71080-0023-4 17 mL in 1 CARTON; Type 0: Not a Combination Product 05/10/2021 5 NDC:71080-0023-5 17 mL in 1 CARTON; Type 0: Not a Combination Product 05/10/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/10/2021 Labeler - GTG WELLNESS CO., LTD. (689458057) Registrant - GTG WELLNESS CO., LTD. (689458057) Establishment Name Address ID/FEI Business Operations Natural Korea Co., Ltd. 688729438 manufacture(71080-0023)