Label: WHITE TEA TINTED MOISTURIZER- white tea tinted moisturizer broad spectrum spf 30 sunscreen cream
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NDC Code(s):
83022-077-01,
83022-077-02,
83022-077-03,
83022-077-04, view more83022-077-05, 83022-077-06, 83022-077-11, 83022-077-12, 83022-077-13, 83022-077-14, 83022-077-15, 83022-077-16
- Packager: GLOW CONCEPT INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 1, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- WHEN USING THIS PRODUCT
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS
Apply liberally 15 minutes before sun exposure • Use a water resistant sunscreen if swimming or sweating
• reapply at least every two hours
• Sun Protection Measures
• Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with
Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
• Limit time in sun, especially from 10 a.m. – 2 p.m.
• Wear long-sleeve shirts, pants, hats, and sunglasses
- OTHER INFORMATION
- CHILDREN UNDER 6 MONTHS
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INACTIVE INGREDIENT SECTION
Water (Aqua), Titanium Dioxide (CI 77891), Potassium Cetyl Phosphate, Glycerin, Ethylhexyl Methoxycrylene, Cetearyl Alcohol, Cetyl Dimethicone, Dimethicone, Isoeicosane, Silica, Sorbitan Sesquioleate, Hydroxyethylacrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 60, Phenoxyethanol, Fragrance, Caprylyl Glycol, Iron Oxide (CI 77492), Hexylene Glycol,
Ethylhexylglycerin, Iron Oxide (CI 77491), Tocopheryl Acetate, Iron Oxide (CI 77499), Tetrahexyldecyl Ascorbate, Camellia Sinensis
(White Tea) Leaf Extract, Punica Granatum (Pomegranate) Extract. - QUESTION AND COMMENTS
- USE
- WHITE TEA TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN (PRINCIPAL DISPLAY PANEL)
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INGREDIENTS AND APPEARANCE
WHITE TEA TINTED MOISTURIZER
white tea tinted moisturizer broad spectrum spf 30 sunscreen creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83022-077 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 7 mg in 1 g Inactive Ingredients Ingredient Name Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) GLYCERIN (UNII: PDC6A3C0OX) BROWN IRON OXIDE (UNII: 1N032N7MFO) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DIMETHICONE (UNII: 92RU3N3Y1O) ISOHEXADECANE (UNII: 918X1OUF1E) POLYSORBATE 60 (UNII: CAL22UVI4M) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) HEXYLENE GLYCOL (UNII: KEH0A3F75J) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDRATED SILICA (UNII: Y6O7T4G8P9) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) FRAGRANCE 13576 (UNII: 5EM498GW35) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17) PUNICA GRANATUM FLOWER (UNII: D9B634V4GP) ISOEICOSANE (UNII: AR294KAG3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) Product Characteristics Color brown (deep plus tint) , brown (Medium Tint) , brown (Deep tint) , brown (LIGHT Tint) , brown (FAIR tint) , brown (medium deep) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83022-077-11 1 in 1 CARTON 10/21/2022 1 NDC:83022-077-01 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:83022-077-12 1 in 1 CARTON 10/21/2022 2 NDC:83022-077-02 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 3 NDC:83022-077-13 1 in 1 CARTON 10/21/2022 3 NDC:83022-077-03 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 4 NDC:83022-077-14 1 in 1 CARTON 10/21/2022 4 NDC:83022-077-04 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 5 NDC:83022-077-15 1 in 1 CARTON 10/21/2022 5 NDC:83022-077-05 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 6 NDC:83022-077-16 1 in 1 CARTON 10/21/2022 6 NDC:83022-077-06 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/21/2022 Labeler - GLOW CONCEPT INC (079853863) Registrant - GLOW CONCEPT INC (079853863)