Label: CELLSKIN CLEAN PINE- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71080-0021-1, 71080-0021-2 - Packager: GTG Wellness 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 December 10, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- PURPOSE
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WARNINGS
For external use only. Flammable. Keep away from heat and Flame.
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Do not use
• in children less than 2 months of age
• on open skin wounds--------------------------------------------------------------------------------------------------------
When using this product keep out of 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.
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Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- CELLSKIN CLEAN PINE LIQUID (BLACK)71080-0021-1
- CELLSKIN CLEAN PINE LIQUID (WHITE)71080-0021-2
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INGREDIENTS AND APPEARANCE
CELLSKIN CLEAN PINE
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0021 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:71080-0021-1 17 mL in 1 CONTAINER; Type 0: Not a Combination Product 12/01/2020 2 NDC:71080-0021-2 17 mL in 1 CONTAINER; Type 0: Not a Combination Product 12/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/01/2020 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(71080-0021)