Label: SUBIR- twinkle essence cream
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Contains inactivated NDC Code(s)
NDC Code(s): 81716-006-01 - Packager: Dream Polymer
- 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 March 30, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
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Warnings
Be careful not to get in your eyes.
If it gets into your eyes, immediately wash if off with clean water several times
Do not eat.
Keep out of reach of children.
Store in a cool place away from direct sunlight.
Follow the recommendations.
After use, if skin irritation such as rash or itching persists, stop use - KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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Inactive ingredients
Water, METHYLPROPANEDIOL, GLYCERIN, BUTYLENE GLYCOL, SODIUM HYALURONATE, 1,2-HEXANEDIOL, CAPRYLYL GLYCOL, CARBOMER, CETYLE THYLHEXANOATE, HYDROXY ACETOPHENONE, NEOPENTYL GLYCOL DICAPRATE, DISODIUM EDTA, ALLANTOIN, STEARIC ACID, GLYCERYL STEARATE, CERAMIDE NP, SUCROSE STEARATE, HEXYL LAURATE, CHOLESTEROL, GLYCOSPHINGOLIPIDS, ETHYLHEXYL GLYCERIN, NELUMBO NUCIFERA FLOWER EXTRACT, MORUS ALBA BARK EXTRACT, SAUSSUREA INVOLUCRATA EXTRACT, LILIUM CANDIDUM FLOWER EXTRACT, HOUTTUYNIA CORDATA EXTRACT, FREESIA ALBA FLOWER EXTRACT, BELLIS PERENNIS(DAISY)FLOWER EXTRACT, LEONTOPODIUM ALPINUM FLOWER EXTRACT, PANAX GINSENG ROOT EXTRACT, BIOTA ORIENTALIS LEAF EXTRACT, CHAMAECYPARIS OBTUSA LEAF EXTRACT, FRAGRANCE
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
SUBIR
twinkle essence creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81716-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 0.1 g in 10 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) METHYLPROPANEDIOL (UNII: N8F53B3R4R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) CAPRYLYL GLYCOL (UNII: 00YIU5438U) NEOPENTYL GLYCOL DICAPRATE (UNII: 77T908SE82) ALLANTOIN (UNII: 344S277G0Z) STEARIC ACID (UNII: 4ELV7Z65AP) CERAMIDE NP (UNII: 4370DF050B) SUCROSE STEARATE (UNII: 274KW0O50M) HEXYL LAURATE (UNII: 4CG9F9W01Q) CHOLESTEROL (UNII: 97C5T2UQ7J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81716-006-01 10 g in 1 CONTAINER; Type 0: Not a Combination Product 03/30/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/30/2021 Labeler - Dream Polymer (695501990) Registrant - Dream Polymer (695501990) Establishment Name Address ID/FEI Business Operations Dream Polymer 695501990 manufacture(81716-006)