Label: SAND CLOUD MINERAL SUNSCREEN FOR FACE- titanium dioxide and zinc oxide lotion
- NDC Code(s): 83081-2056-1
- Packager: Sand Cloud Holdings, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
-
Directions
- shake well prior to use
- apply liberally 15 minutes before sun exposure
- children under 6 months of age: Ask a doctor
- 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 sunglasses
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- Other information
-
Inactive ingredients
Alumina, Aluminum Stearate, Beeswax, C12-15 Alkyl Benzoate, C13-14 Isoparaffin, Caffeine, Camellia Sinensis Leaf (Green Tea) Extract, Caprylyl Glycol, Chlorphenesin, Cyclomethicone, Dimethoxydiphenylsilane, Isostearyl Alcohol, Laureth-7, Lauryl PEG/PPG 18/18 Methicone, Phenoxyethanol, Polyacrylamide, Polyhydroxystearic Acid, Purified Water, Sodium Hyaluronate, Triethoxycaprylylsilane - Questions?
- Sand Cloud Mineral Sunscreen For Face Tube
-
INGREDIENTS AND APPEARANCE
SAND CLOUD MINERAL SUNSCREEN FOR FACE
titanium dioxide and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83081-2056 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 83.4 mg in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength GREEN TEA LEAF (UNII: W2ZU1RY8B0) YELLOW WAX (UNII: 2ZA36H0S2V) CAFFEINE (UNII: 3G6A5W338E) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHLORPHENESIN (UNII: I670DAL4SZ) LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) ALUMINUM OXIDE (UNII: LMI26O6933) HYALURONATE SODIUM (UNII: YSE9PPT4TH) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y) ALUMINUM STEARATE (UNII: U6XF9NP8HM) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) DIMETHOXYDIPHENYLSILANE (UNII: 02QB6788GC) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) WATER (UNII: 059QF0KO0R) CYCLOMETHICONE (UNII: NMQ347994Z) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83081-2056-1 48 g in 1 TUBE; Type 0: Not a Combination Product 06/30/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/30/2023 Labeler - Sand Cloud Holdings, LLC (042484924)
