Label: HANYWIL-DARK SPOT cream
- NDC Code(s): 84867-003-01
- Packager: Jiashen International Trading Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 10, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
WATER
GLYCERIN
PROPYLENE GLYCOL
CAPRYLIC/CAPRIC TRIGLYCERIDE
CETEARYL ALCOHOL
CETEARYL GLUCOSIDE
DIMETHICONE 350
BUTYROSPERMUM PARKII (SHEA) BUTTER
GLYCERYL STEARATE
PORTULACA OLERACEA EXTRACT
CHRYSANTHELLUM INDICUM EXTRACT
PELARGONIUM GRAVEOLENS EXTRACT
MENTHA ARVENSIS LEAF EXTRACT
ALOE BARBADENSIS EXTRACT
SOPHORA ANGUSTIFOLIA ROOT EXTRACT
SQUALANE
TOCOPHERYL ACETATE
1,2-HEXANEDIOL
HYDROXYACETOPHENONE
PHENOXYETHANOL
ETHYLHEXYLGLYCERIN
CARBOMER
DISODIUM EDTA
FRAGRANCE - PURPOSE
- WARNINGS
- STOP USE
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
INSTRUCTIONS
Step 1: Wash your faceand keep it clean.
Step 2: Take an appropriateamount of dark spotcream and apply evenly to the desiredarea, massage gentlyfor 1-2 minutes.
Step 3: Use twice a day, with massage to help absorption, adhere to the use of more than a month the best results.
It is recommended to use it twice a day inthe morning andevening for both menand women. - DOSAGE & ADMINISTRATION
- WHEN USING
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HANYWIL-DARK SPOT
hanywil-dark spot creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84867-003 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN 125 mg in 50 mL INOSITOL (UNII: 4L6452S749) (INOSITOL - UNII:4L6452S749) INOSITOL 1000 mg in 50 mL 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) (3-O-ETHYL ASCORBIC ACID - UNII:6MW60CB71P) 3-O-ETHYL ASCORBIC ACID 100 mg in 50 mL CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) (CENTELLA ASIATICA TRITERPENOIDS - UNII:4YS74Q4G4J) CENTELLA ASIATICA TRITERPENOIDS 99.2 mg in 50 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 1500 mg in 50 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIMETHICONE 350 (UNII: 2Y53S6ATLU) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) CHRYSANTHELLUM INDICUM TOP (UNII: STJ856D1Z0) CARBOMER (UNII: 0A5MM307FC) FRAGRANCE 13576 (UNII: 5EM498GW35) GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) PORTULACA OLERACEA LEAF (UNII: 9JW9D9JGHZ) PELARGONIUM GRAVEOLENS LEAF OIL (UNII: 5Q1I94P4WG) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ALOE BARBADENSIS LEAF EXTRACT (UNII: ZY81Z83H0X) SQUALANE (UNII: GW89575KF9) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) EDETATE DISODIUM (UNII: 7FLD91C86K) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) CETEARYL ALCOHOL (UNII: 2DMT128M1S) MENTHA ARVENSIS LEAF (UNII: A4IWO4DDZ9) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84867-003-01 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/10/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 11/10/2024 Labeler - Jiashen International Trading Co., Ltd. (989067943)

