Label: ENASKIN DARK SPOT CORRECTOR- niacinamide, 3-o-ethyl ascorbic acid, alpha-arbutin, panthenol liquid
- NDC Code(s): 82898-001-01, 82898-001-02
- Packager: EnaSkin LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 11, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Active ingredients
Purpose
Niacinamide 3%.......................................................................................Reduce Dark Spots
3-o-ethyl Ascorbic Acid 2%.........................................................................Reduce Dark Spots
Alpha-Arbutin 1%......................................................................................Reduce Dark Spots
Panthenol 0.5%.........................................................................................Reduce Dark Spots - PURPOSE
- Uses
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Warnings
For external use only
Do not use on damaged or broken skin. Do not use on individuals aged 12 and under.
When using this product avoid contact with eyes.
Please test this serum on a small patch of your dark spot if it is your first time using this serum.
Stop and ask a doctor if irritation or allergic reactions develop.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of accidental ingestion, seek medical advice immediately or
contact a Poison Control Center right away. - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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Inactive ingredients
Aqua, Propylene Glycol, Glycerin, Peg/ppg-17/6 Copolymer, Betaine, Butylene Glycol, 1,2-Hexanediol, Hydroxyacetophenone, Xanthan Gum, Dipotassium Glycyrrhizate, Allantoin, Chlorphenesin, Salicylic Acid, Sodium Hydroxide, Sodium Hyaluronate, Dendrobium Nobile Extract,
Macrocystis Pyrifera (Kelp) Extract, Chenopodium Quinoa Seed Extract, Hydroxyphenyl Propamidobenzoic Acid, Phospholipids, Tocopheryl Acetate, Salvia Miltiorrhiza Root Extract, Glycyrrhiza Uralensis (Licorice) Root Extract, Scutellaria Baicalensis Root Extract, Rhodiola Crenulata
Root Extract, Eugenia Caryophyllus (Clove) Bud Extract, Polygala Tenuifolia Root Extract, Centella Asiatica Extract, Alisma Orientale Extract, Superoxide Dismutase, Trehalose, Punica Granatum Fruit Extract, Morinda Citrifolia Fruit Extract, Rosa Multiflora Root Extract, Castanea Sativa (Chestnut) Leaf Extract, Lactic Acid, CI 19140, CI 15985 - Questions or comments?
- Product label
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INGREDIENTS AND APPEARANCE
ENASKIN DARK SPOT CORRECTOR
niacinamide, 3-o-ethyl ascorbic acid, alpha-arbutin, panthenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82898-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 3 g in 100 mL 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) (3-O-ETHYL ASCORBIC ACID - UNII:6MW60CB71P) 3-O-ETHYL ASCORBIC ACID 2 g in 100 mL ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN 1 g in 100 mL PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259) BETAINE (UNII: 3SCV180C9W) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) XANTHAN GUM (UNII: TTV12P4NEE) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) ALLANTOIN (UNII: 344S277G0Z) CHLORPHENESIN (UNII: I670DAL4SZ) SALICYLIC ACID (UNII: O414PZ4LPZ) SODIUM HYDROXIDE (UNII: 55X04QC32I) HYALURONATE SODIUM (UNII: YSE9PPT4TH) DENDROBIUM NOBILE WHOLE (UNII: 1Y5P4E7CC6) MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4) CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X) HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN) GLYCYRRHIZA URALENSIS ROOT (UNII: 42B5YD8F0K) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) RHODIOLA CRENULATA ROOT (UNII: G7TMD86VH5) CLOVE (UNII: K48IKT5321) POLYGALA TENUIFOLIA ROOT (UNII: 5S7W573MTU) CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) ALISMA PLANTAGO-AQUATICA SUBSP. ORIENTALE WHOLE (UNII: Z77940VG9A) SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE) (UNII: W2T4YRA9AD) TREHALOSE (UNII: B8WCK70T7I) POMEGRANATE (UNII: 56687D1Z4D) NONI FRUIT (UNII: 7829X3G2X5) ROSA MULTIFLORA ROOT (UNII: 6X8YF4S72T) CASTANEA SATIVA LEAF (UNII: IV3S2HH53G) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) PORACTANT ALFA (UNII: KE3U2023NP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82898-001-01 1 in 1 BOX 04/10/2023 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:82898-001-02 1 in 1 BOX 04/10/2023 2 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/10/2023 Labeler - EnaSkin LLC (118723349)
