Label: GZE INDIAN HEALING CLAY- bentonite powder
- NDC Code(s): 83566-042-01
- Packager: Guangzhou Yilong Cosmetics Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 7, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
-
INDICATIONS & USAGE
Mix clay with equal parts of raw apple cider vinegar and/or water.Use anon-metal bow and utensil. Stir the mixture well to a smooth paste.Add more clay or liquid as needed.Apply1/8 to 1/4 into the face or other area. Let it dry for 5-10 min for delicate skin and 15-20 min for normal skin. You will feel a pulling and tightening sensation,Feel your face pulsate! Remove clay by washing with warm water. Slightredness of the skin is normal and will disappearin about 30 min.Removes impurities and dirt from the pores. Deep pore cleansing.Use it once per week for the family. For external use only.
- WARNINGS
- STOP USE
- DO NOT USE
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
Mix clay with equal parts of raw apple cider vinegar and/or water.Use anon-metal bow and utensil. Stir the mixture well to a smooth paste.Add more clay or liquid as needed.Apply1/8 to 1/4 into the face or other area. Let it dry for 5-10 min for delicate skin and 15-20 min for normal skin. You will feel a pulling and tightening sensation,Feel your face pulsate! Remove clay by washing with warm water. Slightredness of the skin is normal and will disappearin about 30min.Removes impurities and dirt from the pores. Deep pore cleansing.Use it once per week for the family. For external use only.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GZE INDIAN HEALING CLAY
bentonite powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-042 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENTONITE (UNII: A3N5ZCN45C) (BENTONITE - UNII:A3N5ZCN45C) BENTONITE 100 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-042-01 100 g in 1 BAG; Type 0: Not a Combination Product 12/20/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 12/20/2023 Labeler - Guangzhou Yilong Cosmetics Co.,Ltd. (712647107) Establishment Name Address ID/FEI Business Operations Guangzhou Yilong Cosmetics Co.,Ltd. 712647107 manufacture(83566-042)
