Label: AMBLING PLANT PROBIOTICS AQUA ROLE MOISTURIZING- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 73456-020-01, 73456-020-02 - Packager: Amtixbio 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 February 16, 2022
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
Water, Glycerin, Butylene Glycol, Squalane, Olea Europaea (Olive) Fruit Oil, Glyceryl Stearate, PEG-100 Stearate, Trehalose, Limnanthes Alba (Meadowfoam) Seed Oil, Polyacrylate-13, Polyisobutene, Polysorbate 20, Sorbitan Isostearate, Palmitic Acid, Stearic Acid, Pediococcus Ferment Extract, Butyrospermum Parkii (Shea) Butter, Glyceryl Stearate, Cetearyl Alcohol, Fragrance, Sodium Hyaluronate, Disodium EDTA, Argania Spinosa Kernel Oil, Betaine, Tocopherol, Helianthus Annuus (Sunflower) Seed Oil, Vitis Vinifera (Grape) Seed Oil, Butylene Glycol, Hedera Helix (Ivy) Extract, Butylene Glycol, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Rose Flower Oil, Pelargonium, Portulaca Oleracea Extract, Salix Alba (Willow) Bark Extract, Lactobacillus/Soybean Ferment Extract, Cinnamomum Cassia Bark Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Butylene Glycol, Moringa Oleifera Seed Oil, Ceramide NP, Phytosphingosine, Hydrogenated Lecithin, Oenothera Biennis (Evening Primrose) Oil, Butylene Glycol, Imperata Cylindrica Root Extract, Opuntia Ficus-Indica Stem Extract, Adansonia Digitata Seed Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Ascorbic Acid, Olea Europaea (Olive) Fruit Oil, Lavandula Angustifolia (Lavender) Oil, Eucalyptus Globulus Leaf Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Citrus Limon (Lemon) Peel Oil, Citrus Medica Vulgaris Peel Oil, Cananga Odorata Flower Oil, Aniba Rosaeodora (rosewood) Wood Oil, Citrus Nobilis (Mandarin Orange) Peel Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Salvia Sclarea (Clary) Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Graveolens Flower Oil, Anthemis Nobilis Flower Oil, Illicium Verum (Anise) Fruit/Seed Oil, Citrus Aurantium Dulcis (Orange) Flower Oil, Rose Flower Oil, Jasminum Officinale (Jasmine) Oil, Myristic Acid, Arachidic Acid, Lauric Acid, Limonene, Linalool, hexyl Cinnamal, Citronellol
- PURPOSE
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WARNINGS
1. Consult a specialist if you have abnormal symptoms or side effects such as red spots, swelling, or itching in the area of use due to direct sunlight during or after using cosmetics.
2. Do not use this product in areas with scratches, eczema, or dermatitis.
3. Storage and Handling Precautions
1) Always close the cap after use.
2) Please keep out of reach of infants and children.
3) Please keep it away from direct sunlight.4. If an infant or a child takes cosmetics accidently, consult a medical doctor immediately and take emergency measures.
5. Do not use it for infants under the age of three.
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AMBLING PLANT PROBIOTICS AQUA ROLE MOISTURIZING
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73456-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.00 g in 50 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73456-020-02 1 in 1 CARTON 10/01/2019 1 NDC:73456-020-01 50 mL 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 10/01/2019 Labeler - Amtixbio Co., Ltd. (694464882) Registrant - Amtixbio Co., Ltd. (694464882) Establishment Name Address ID/FEI Business Operations IMINE CO., LTD. 557816813 manufacture(73456-020)