Label: BURZANGMURY GOLD TREATMENT- glycerin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 58906-2001-1 - Packager: Dae Deok bio Inc
- 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 August 16, 2013
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Cetrimonium Chloride, cetyl alcohol, cyclopentasiloxane, dimethicone, cocamidoproplyl Betaine, caprlic/capric triglyceride, glyceryl stearate,Dicetyldimonium Chloride, Cetearyl alcohol, glycerin, 1,2-hexandiol, caprylyl Glycol, butylene glycol, À̴нº¿¸ÅÃßÃâ¹°, ginseng extract, perfume, polyquaternium-10, Hydroxyethylcellulose, panthenol, tocopheryl acetate, disodium EDTA
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
- Stop using the treatment if sensitivities as below occurs and consult with dermatologist
- sensitivities such as red marks, intumescence, urtication, irritation during use
-Have sensitivities as above on applied part by direct sun ray
- Do not use the shampoo on the part of scar, eczema, dermatitis and etc.
- Wash away immediately if shampoo get in our eyes.
- throughly rinse after use. Improper washing may cause hair loss, decolor of your hair.
- Storage and handling
- Close lid after use.
- Do not store at high and low temperatures and avoid sunlight.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BURZANGMURY GOLD TREATMENT
glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58906-2001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 0.01 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58906-2001-1 150 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 08/16/2013 Labeler - Dae Deok bio Inc (688809847) Registrant - Dae Deok bio Inc (688809847) Establishment Name Address ID/FEI Business Operations Dae Deok bio Inc 688809847 manufacture(58906-2001)