Label: MEFACTORY SUPER DEEP CLEANSING FOA M- witch hazel cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70908-200-01 - Packager: MeFactory Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 2, 2018
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Stearic Acid, Glycerin, Lauric Acid, Potassium Hydroxide, Myristic Acid, Beeswax, Polysorbate 20, Glycol Stearate, 1,2-Hexanediol, Cocamidopropyl Betaine, PEG-100 Stearate, Glyceryl Stearate, Hydroxyacetophenone, Hexylene Glycol, Ethylhexyl Methoxycinnamate , Fragrance, Disodium EDTA, Butylene Glycol, Pentylene Glycol, Illite, Kaolin, CI 14700 , Citrus Paradisi (Grapefruit) Fruit Extract, Citrus Limon (Lemon) Fruit Extract, CI 19140
- PURPOSE
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WARNINGS
Warnings: For external use only 1. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, red spot, itchy skin or rash 2) Applied skin area has the above reaction from direct sun. 2. Do not use on irritated skin, cuts, or other infected skin areas. 3. Avoid direct contact with eyes
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- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEFACTORY SUPER DEEP CLEANSING FOA M
witch hazel creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70908-200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Witch Hazel (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34) Witch Hazel 0.001 g in 120 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70908-200-01 120 g in 1 TUBE; Type 0: Not a Combination Product 12/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 12/01/2017 Labeler - MeFactory Co., Ltd. (689840967) Registrant - MeFactory Co., Ltd. (689840967) Establishment Name Address ID/FEI Business Operations CNF CO.,LTD. 689852175 manufacture(70908-200)