Label: WHITENING TURMERIC OIL oil
- NDC Code(s): 84423-003-01
- Packager: Guangzhou Kadiya Biotechnology Co. Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 27, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Inactive ingredients
- PURPOSE
- WARNINGS
- Instructions for use
- Dosage
- Warning
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PRINCIPAL DISPLAY PANEL
WHITENING Turmeric OIL
1.Purpose
For soothing, moisturizing, nourishing and brightening the skin
2. Warning
1. )Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2.) For external use only, avoid contact with eyes when use
3. )Keep out of reach of children
3 Active ingredints
Kojic acid0.2%
ZINGIBER OFFICINALE ROOT EXTRACTO.3%
OLEA EUROPAEA FRUIT EXTRACT2.8%
4.Inactive ingredients: MINERAL OIL, ISOPROPYL MYRISTATE, DIMETHICONE, ISOPROPYL PALMITATE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, SQUALANE, WATER, PHENOXYETHANOL,ETHYLHEXYLGLYCERIN PARFUM, PROPYLPARABEN, CI17200, CI 45370
5.Instructions for use
Apply proper amount to face, back and other parts. Gently massage to allow the skin to absorb.
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INGREDIENTS AND APPEARANCE
WHITENING TURMERIC OIL
whitening turmeric oil oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-003 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID 0.4 mg in 200 mg OLIVE OIL (UNII: 6UYK2W1W1E) (OLIVE OIL - UNII:6UYK2W1W1E) OLIVE OIL 5.6 mg in 200 mg Inactive Ingredients Ingredient Name Strength GINGER (UNII: C5529G5JPQ) D&C RED NO. 33 (UNII: 9DBA0SBB0L) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) SOLVENT RED 72 (UNII: 7MF02AWG95) SQUALANE (UNII: GW89575KF9) JOJOBA OIL (UNII: 724GKU717M) PHENOXYETHANOL (UNII: HIE492ZZ3T) DIMETHICONE 350 (UNII: 2Y53S6ATLU) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) PROPYLPARABEN (UNII: Z8IX2SC1OH) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-003-01 200 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/28/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/28/2024 Labeler - Guangzhou Kadiya Biotechnology Co. Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-003)