Label: DIAMOND GLOW DARK SPOT CORRECTOR FACE CREAM- diamondglowdarkspotcorrectorface cream cream, augmented
- NDC Code(s): 84423-048-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 28, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PURPOSE
-
INACTIVE INGREDIENT
AQUA，GLYCERIN，MINERAL OIL，DIMETHICONE，POLYSORBATE 60，PALMITIC ACID，ETHOXYDIGLYCOL，STEARIC ACID，LAURIC/MYRISTIC/PALMITIC/STEARIC GLYCERIDES，STEARYL ALCOHOL，GLYCERYL STEARATE，HYDROGENATED LECITHIN，TITANIUM DIOXIDE，CETYL ALCOHOL，TRIETHANOLAMINE，LANOLIN，PHENOXYETHANOL，ALLANTOIN，METHYLPARABEN，TRANEXAMIC ACID，YEAST FERMENT EXTRACT，MYRISTIC ACID，PROPYLPARABEN，FRAGRANCE，LAURIC ACID，ALUMIN， MYRISTYL ALCOHOL，ARACHIDYL ALCOHOL，CI 19140，SODIUM CHLORIDE，CI 15985
- WARNINGS
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INDICATIONS & USAGE
Diamond Glow Dark Spot Corrector, infused Amla and Dandelion extracts, synergystically work together to naturally lighten unwanted spots and provide antioxident protection against environemental aggressors. This skin-correcting cream can help fade pigmentation from dark elbows, knuckles, spots, marks and post-acne blemishes helping to promote and maintain a more even, unified complexion.
- DOSAGE & ADMINISTRATION
- KEEP OUT OF REACH OF CHILDREN
- ACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
Active Ingredients
ALPHA-ARBUTIN1%
ASCORBIC ACID0.5%
NIACINAMIDE 2%
TARAXACUM OFFICINALE EXTRACT0.5%
Uses：
For brightening the face and moisturising the skin.
The storage method：
Store sealed in a cool place and out of sunlight
Warning.
1、For external use only, avoid contact with eyes when used
2、Keep out of reach of children
Inactive ingredients：
AQUA，GLYCERIN，MINERAL OIL，DIMETHICONE，POLYSORBATE 60，PALMITIC ACID，ETHOXYDIGLYCOL，STEARIC ACID，LAURIC/MYRISTIC/PALMITIC/STEARIC GLYCERIDES，STEARYL ALCOHOL，GLYCERYL STEARATE，HYDROGENATED LECITHIN，TITANIUM DIOXIDE，CETYL ALCOHOL，TRIETHANOLAMINE，LANOLIN，PHENOXYETHANOL，ALLANTOIN，METHYLPARABEN，TRANEXAMIC ACID，YEAST FERMENT EXTRACT，MYRISTIC ACID，PROPYLPARABEN，FRAGRANCE，LAURIC ACID，ALUMIN， MYRISTYL ALCOHOL，ARACHIDYL ALCOHOL，CI 19140，SODIUM CHLORIDE，CI 15985
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INGREDIENTS AND APPEARANCE
DIAMOND GLOW DARK SPOT CORRECTOR FACE CREAM
diamondglowdarkspotcorrectorface cream cream, augmentedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-048 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 1 g in 50 mL ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN 0.5 g in 50 mL ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 0.25 g in 50 mL TARAXACUM OFFICINALE ROOT (UNII: 9DE5YCO0RU) (TARAXACUM OFFICINALE ROOT - UNII:9DE5YCO0RU) TARAXACUM OFFICINALE ROOT 0.25 g in 50 mL Inactive Ingredients Ingredient Name Strength STEARYL ALCOHOL (UNII: 2KR89I4H1Y) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) LAURIC ACID (UNII: 1160N9NU9U) ALUMINUM OXIDE (UNII: LMI26O6933) PALMITIC ACID (UNII: 2V16EO95H1) METHOXYDIGLYCOL (UNII: 465DDJ8G8K) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ALLANTOIN (UNII: 344S277G0Z) PROPYLPARABEN (UNII: Z8IX2SC1OH) MYRISTYL ALCOHOL (UNII: V42034O9PU) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) SODIUM CHLORIDE (UNII: 451W47IQ8X) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) MINERAL OIL (UNII: T5L8T28FGP) STEARIC ACID (UNII: 4ELV7Z65AP) POLYSORBATE 60 (UNII: CAL22UVI4M) TROLAMINE (UNII: 9O3K93S3TK) METHYLPARABEN (UNII: A2I8C7HI9T) MYRISTIC ACID (UNII: 0I3V7S25AW) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) TRANEXAMIC ACID (UNII: 6T84R30KC1) DIMETHICONE (UNII: 92RU3N3Y1O) CETYL ALCOHOL (UNII: 936JST6JCN) LANOLIN (UNII: 7EV65EAW6H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-048-01 50 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/29/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 09/29/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-048)