Label: INCELLDERM COCKTAIL AQUA BB- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72650-050-01, 72650-050-02 - Packager: Riman Co., Ltd.
- 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 June 29, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Centella Asiatica Leaf Water, Caprylic/Capric Triglyceride, Cetylethyl Hexanoate, Titanium Dioxide, Propylene Glycol , Dimethicone, Hexyl Laurate, Cetyl PEG/PPG-10/1 Dimethicone, 1,2-Hexanediol, Glycerin, Magnesium Sulfate, Sorbitan Sesquioleate, Butylene Glycol, Glutathione, Anemarrhena Asphodeloides Root Extract, Hydrogenated Polyisobutene, Oligopeptide-91 rh-Oligopeptide-1, Palmitoyl Tripeptide-5, sh-Polypeptide-1, Citrus Aurantifolia (Lime) Fruit Extract, Hydrogenated Lecithin, Glycine Soja (Soybean) Sterols, Hydroxydecyl Ubiquinone, Panthenol, Lavandula Angustifolia (Lavender) Oil, Hydroxyethylcellulose, Zinc Stearate, Microcrystalline Wax, Allantoin, Tocopheryl Acetate, Aluminum Hydroxide, Silica Dimethyl Silylate, Iron Oxide (CI 77492), Iron Oxide (CI 77491), Iron Oxide (CI 77499), Talc, Triethoxycaprylylsilane, Disodium EDTA
- PURPOSE
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WARNINGS
1. Consult a physician if red spots, swollenness, itchiness, or any other adnormal symptoms or side effects develops on the applied area during or after use or under direct sunlight.
2. Do not use on wound, etc.
3. Precautions for handling and storage
a) Keep out of the reach of children
b) Avoid direct sunlight - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INCELLDERM COCKTAIL AQUA BB
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72650-050 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.60 g in 30 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 30 g Inactive Ingredients Ingredient Name Strength CENTELLA ASIATICA LEAF (UNII: 6810070TYD) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72650-050-02 1 in 1 CARTON 03/01/2019 1 NDC:72650-050-01 30 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2019 Labeler - Riman Co., Ltd. (694893735) Registrant - Riman Co., Ltd. (694893735) Establishment Name Address ID/FEI Business Operations HANSOLBIOTECH 694455165 manufacture(72650-050)
