Label: DARK KNUCKLEE SERUM oil
- NDC Code(s): 84423-004-01
- Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 27, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVIE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- WARNING
- INSTRUCTIONS FOR USE
- DOSAGE
- Warning
- USAGE
-
PACKAGE LABEL
Terminal white secret SERUM for dark knuckleelbow & knee
1. Active Ingredients
GLUTATHIONE0.3%
Alpha Arbutin0.5%
SALICYLIC ACID 0.5%2.Purpose
For Removal of Pigmented Spots3.Inactive ingredients:
ETHYLHEXYL PALMITATE, ISONONYL ISONONANOATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, AROMA, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE4.Warning
1.Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
2. For external use only, avoid contact with eyes when used.
3. Keep out of reach of children.5.Instructions for use
Apply to affected area at night only. Clean and dry your skin, apply1 to 2 drops of serum with your fingertips in motions until absorbed
-
INGREDIENTS AND APPEARANCE
DARK KNUCKLEE SERUM
dark knucklee serum oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84423-004 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN 0.25 mg in 50 mg GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 0.25 mg in 50 mg SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.15 mg in 50 mg Inactive Ingredients Ingredient Name Strength ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ETHYLHEXYL PALMITATE (UNII: 2865993309) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84423-004-01 50 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/28/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 06/28/2024 Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913) Establishment Name Address ID/FEI Business Operations Guangzhou Kadiya Biotechnology Co., Ltd. 713172913 manufacture(84423-004)