Label: BODYHOLIC RED POTION HAIR AND BODY MIST- glycerin spray
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Contains inactivated NDC Code(s)
NDC Code(s): 70908-110-01, 70908-110-02 - Packager: MeFactory Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 13, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, PEG-40 Hydrogenated Castor Oil, Alcohol, Fragrance, Phenoxyethanol, Erythritol, Butyl Methoxydibenzoylmethane, Disodium EDTA, Sodium Citrate, Citric Acid, Butylene Glycol, Centella Asiatica Extract, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Onsen-Sui
- 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 spots, 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 area. 3. Avoid contact with eyes
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BODYHOLIC RED POTION HAIR AND BODY MIST
glycerin sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70908-110 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 0.5 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70908-110-02 1 in 1 CARTON 04/01/2017 1 NDC:70908-110-01 50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/01/2017 Labeler - MeFactory Co., Ltd. (689840967) Registrant - MeFactory Co., Ltd. (689840967) Establishment Name Address ID/FEI Business Operations MeFactory Co., Ltd. 689840967 manufacture(70908-110)