Label: BEAUTYTURESS TINTED SUNSCREEN emulsion
- NDC Code(s): 84753-001-01
- Packager: Guangdong Bisutang Biotechnology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 28, 2024
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- Active Ingredient
- PURPOSE
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DOSAGE & ADMINISTRATION
Directions
Apply liberally/generously (and evenly) 15 minutes before sun exposure
For use on children less than 6 months of age, consult a health care practitioner
Reapply
At least every 2 hours
After 80 minutes of swimming or sweating
Immediately after towel drying
after eating or drinkingMode d'emploi
Appliquer généreusement (et uniformément) 15 minutes avant l'exposition au soleil
Pour les enfants agés de moins de 6 mois, consulter un praticien de soins de santé
Appliquer denouveau:
au moins toutes les 2 heures
aprés 80 minutes de baignade ou aprés avoir mangé ou bu. - WHEN USING
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WARNINGS
Risk InformationFor external use only
Mention de risquesPour usage externe seulement
Do not use on damaged or broken skin.
Ne pas utiliser sur la peau endommagée ou avec des lésions
If rash occurs, discontinue use and consult a health care practitioner.
En présence d'une éruption cutanée, cesser l'utilisation et consulter un praticien de soins de santé
When using this product keep out of eyes. Rinse with water to remove.
Eviter tout contact avec les yeux. Rincer a l'eau le cas échéant
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Tenir hors de portée des enfants
En cas d'ingestion, consulter un médecin ou appeler un centre antipoison immédiatement. -
INDICATIONS & USAGE
Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including
Limit time in the sun, especially from 10 a.m.-2 p.m.
Wear long-sleeved shirts, pants, hats, and sun glasses.Mesures de protection contre le soleil Passer du temps au soleil augmente le risque de cancer de la peau et de vieillissement prématuré de la peau. Afin de diminuer ce risque, il convient d'utiliser réeguliérement un écran solaire avec un F.P.S. a large spectre d'au moins 15 et d'appliquer d'autres mesures de protection contre le soleil, telles que
limiter le temps passé au soleil notamment entre 10 et 14 heures
porter des chemises a manches longues, des pantalons, un chapeau et des lunettes de soleil. - KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Aloe Barbadensis Leaf Juice, C12-15 Alky Benzoate, Caprylic/Capric Triglyceride, Glyceryi Stearate, Helianthus Annuus(Sunflower) Seed Oil, Ricinus Communis (Castor) Seed Oil, Beeswax, Oryza Sativa (Rice) Bran Wax, Sorbitan Sesquioleate，glycerin, Cetyi Alcohol, Stearyl Alcohol, Magnesium Aluminum silicate, Butyrospermum Parki (Shea) Butter, Camellia Sinensis flower extract, Ilex Paraguariensis Leaf Extract, Rosa Canina Fruitoil, Tocopheryi Acetate, Carthamus Tinctorius (Safflower) Seed, Oilrubus Idaeus (Raspberry) Fruit Extract, Squalane, Xanthan Gum, Propanediol, Ethylhexy glycerin, Potassium Sorbate, Fragrance
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BEAUTYTURESS TINTED SUNSCREEN
beautyturess tinted sunscreen emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84753-001 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 50 mg in 50 mg TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 50 mg in 50 mg Inactive Ingredients Ingredient Name Strength SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) CASTOR OIL (UNII: D5340Y2I9G) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCERIN (UNII: PDC6A3C0OX) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SHEA BUTTER (UNII: K49155WL9Y) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) XANTHAN GUM (UNII: TTV12P4NEE) SUNFLOWER OIL (UNII: 3W1JG795YI) YELLOW WAX (UNII: 2ZA36H0S2V) RICE BRAN (UNII: R60QEP13IC) SAFFLOWER SEED (UNII: 8FCL6A31TX) ALOE VERA LEAF (UNII: ZY81Z83H0X) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) CETYL ALCOHOL (UNII: 936JST6JCN) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) BRASSICA NAPUS SUBSP. NAPUS SEED (UNII: UA8V5JBH7U) SQUALANE (UNII: GW89575KF9) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) .GAMMA.-TOCOPHEROL, DL- (UNII: ECY0XG64DO) PROPANEDIOL (UNII: 5965N8W85T) MYRISTICA FRAGRANS WHOLE (UNII: MF7T8BM40A) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84753-001-01 50 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 09/23/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/23/2024 Labeler - Guangdong Bisutang Biotechnology Co., Ltd. (447075429) Registrant - Guangdong Bisutang Biotechnology Co., Ltd. (447075429) Establishment Name Address ID/FEI Business Operations Guangdong Bisutang Biotechnology Co., Ltd. 447075429 manufacture(84753-001)
