Label: WHITENING CREAM cream
- NDC Code(s): 84117-007-01, 84117-007-02
- Packager: Shenzhen Hengkaifeng Commerce and Trade Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 28, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Use
-
Warnings
Keep out of reach of children. For external use only. Before
using,test for sensitivity on a small area of skin.
Do not use on damaged skin. Use only as directed. Avoid
contact with eyes.Rinse with warm water to remove. Stop
use and consult your physician it rash occurs. Do not ingest.
lf swallowed, get medical help or contact a Poison Control
Center right away! Do not use if safety seal is breken or
missing. Store in a cool, dry place. -
When Using
When using this product keep out of
eyes, ears, and mouth, In case of contact
with eyes,rinse eyes thoroughly with
water. Stop use and ask a doctor if
irritation or rash occurs. These may be
signs of a serious condition.Keep out of
reach of children. If swallowed, get
medical help or contact a Poison Control
Center right away. - Keep Out Of Reach Of Children
- Directions Of Safe Use:
-
Inactive ingredients
Water, Sunflower Oil, Esters of Caprylic and Capric Acids,
Trideceth-6, Aloe Vera, Niacinamide, Glycyrrhiza Glabra
(Licorice) Extract, Morus Alba Root (Mulberry) Extract,
Hydrolyzed Oat Protein Ethyl Ascorbic Acid,
Hyaluronic Acid, Phenoxyethanol, Green Tea Extract,
Tetrapeptide-21, Collagen, Tocopherol, Potassium Sorbate,
Citric Acid, Lemon Essential Oil. - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
WHITENING CREAM
whitening cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84117-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN 2 g in 100 mL Inactive Ingredients Ingredient Name Strength POTASSIUM SORBATE (UNII: 1VPU26JZZ4) GREEN TEA LEAF (UNII: W2ZU1RY8B0) ATELOCOLLAGEN (UNII: 8WBS95X4J5) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LEMON OIL (UNII: I9GRO824LL) TOCOPHEROL (UNII: R0ZB2556P8) TETRAPEPTIDE-21 (UNII: 179JUC43HU) WATER (UNII: 059QF0KO0R) SUNFLOWER OIL (UNII: 3W1JG795YI) OCTANOIC ACID (UNII: OBL58JN025) TRIDECETH-6 (UNII: 3T5PCR2H0C) ALOE VERA LEAF (UNII: ZY81Z83H0X) NIACINAMIDE (UNII: 25X51I8RD4) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) MORUS ALBA ROOT (UNII: CST1G9BZGD) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) HYALURONIC ACID (UNII: S270N0TRQY) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84117-007-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/29/2024 2 NDC:84117-007-02 50 mL in 1 CANISTER; Type 0: Not a Combination Product 04/29/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 04/29/2024 Labeler - Shenzhen Hengkaifeng Commerce and Trade Co., Ltd (444722774) Establishment Name Address ID/FEI Business Operations Shenzhen Hengkaifeng Commerce and Trade Co., Ltd 444722774 manufacture(84117-007) , label(84117-007)
