NDC | 60778-010-01 |
Set ID | 4d78a6bb-2d1f-4ca6-a6f5-37269eb3a4a2 |
Category | HUMAN OTC DRUG LABEL |
Packager | Lycoris Co., Ltd. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Cyclopentasiloxane, Butylene glycol, Isoamyl p-methoxycinnamate, Cetyl PEG/PPG-10/1 Dimethicone, Betaine, Cetyl ethylhexanoate, Polysorbate 60, Dimethicone, Sodium chloride, Sodium hyaluronate, PEG-40 stearate, Iron oxides, Bentonite, Talc, Stearic acide, Phenoxyethanol, Methylparaben, Ethylparaben, Butylparaben, Propylparaben, Isobutylparaben, Tocopheryl acetate, Perfume, Rubus hirsutus fruit/leaf extract, Camellia Japonica Ovary Powder, Centella asiatica extract, Lavandula angustifolia (Lavender) extract, Glycyrrhiza glabra (Licorice) root extract, Triticum vulgare (Wheat) flour lipids, Allantoin, Lysine HCL, Disodium EDTA, Proline, Sodium ascorbyl phosphate, Linum usitatissimum (Linseed) seed extract, Hibiscus esculentus fruit extract, Aloe barbadensis leaf juice, Arctium lappa root extract, Hibiscus mutabilis flower extract, Corchorus olitorius leaf extract, Dimethyl sulfone
- PURPOSE
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WARNINGS
Warnings: 1. In case of having following symptoms after using this, you’re advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problem such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In the case of getting it into your eyes, you have to wash it immediately.
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
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DOSAGE AND ADMINISTRATION
Dosage and administration: Apply after washing face. Take a small amount of cream about 1.0-1.5g on to the fingertips and gently massage over the entire face.(cheeks, nostrils, corners, forehead, and the around of eyes, even your hands) Blot face lightly with tissue, and may sleep without washing it.
- PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LYCORIS RUBUS BRIGHTENING BB SPF40 PA PLUS PLUS
octinoxate, titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60778-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 3 mg in 40 mL Titanium dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium dioxide 2 mg in 40 mL Zinc oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 2 mg in 40 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60778-010-01 40 mL in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 09/01/2013 Labeler - Lycoris Co., Ltd. (688301521) Registrant - Lycoris Co., Ltd. (688301521) Establishment Name Address ID/FEI Business Operations Lycoris Co., Ltd. 688301521 manufacture(60778-010)