Label: YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- HONEY GLOW- your name mineral sheer tint cream
- NDC Code(s): 59735-174-01
- Packager: Mana Product, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 4, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USE
- WARNINGS
-
DIRECTIONS
Apply liberally 15 minutes before sun exposure.
Use water resistant sunscreen if swimming or sweating.Reapply at least every 2 hours.
Children under 6 months: ask a doctor.
Sun Protection Measures: Spending time in the sun increases risk of skin cancer and early 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 10:00 am - 2:00 pm. Wear long sleeved shirts, pants, hats and sunglasses. - OTHER INFORMATION
- INDICATIONS & USAGE
-
INACTIVE INGREDIENT
Water, Cyclopentasiloxane, Butylene Glycol, Titanium Dioxide, Zinc Oxide, Octyldodecyl Neopentanoate, PEG/PPG-18/18 Dimethicone, Dimethicone, Tocopherol, Tetrahexyldecyl Ascorbate, Retinyl Palmitate, Camellia Sinensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ginkgo Biloba Leaf Extract, Panax Ginseng Root Extract, Octyldodecanol, Boron Nitride, Dextrin Palmitate, Palmitic Acid, Methicone, Stearic Acid, Magnesium Chloride, Potassium Chloride, Sodium Chloride, Zinc Chloride, Magnesium Ascorbyl Phosphate, Sodium Hyaluronate, Phytantriol, Glycerin, Triethoxycaprylylsilane, Lysine, Aluminum Hydroxide, Disodium EDTA, Hexylene Glycol, Potassium Sorbate, Sodium Dehydroacetate, Caprylyl Glycol, Phenoxyethanol
MAY CONTAIN (+/-):
Mica, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499)
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- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20- HONEY GLOW
your name mineral sheer tint creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59735-174 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 5 g in 30 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5 g in 30 mL Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) TOCOPHEROL (UNII: R0ZB2556P8) ASIAN GINSENG (UNII: CUQ3A77YXI) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) METHICONE (20 CST) (UNII: 6777U11MKT) STEARIC ACID (UNII: 4ELV7Z65AP) POTASSIUM CHLORIDE (UNII: 660YQ98I10) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) BORON NITRIDE (UNII: 2U4T60A6YD) MAGNESIUM CHLORIDE (UNII: 02F3473H9O) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CHAMOMILE (UNII: FGL3685T2X) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) CAPRYLYL GLYCOL (UNII: 00YIU5438U) MICA (UNII: V8A1AW0880) PALMITIC ACID (UNII: 2V16EO95H1) WATER (UNII: 059QF0KO0R) GINKGO (UNII: 19FUJ2C58T) OCTYLDODECANOL (UNII: 461N1O614Y) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) HYALURONIC ACID (NON-ANIMAL STABILIZED) (UNII: B7SG5YV2SI) PHYTANTRIOL (UNII: 8LVI07A72W) DIMETHICONE (UNII: 92RU3N3Y1O) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3) EDETATE DISODIUM (UNII: 7FLD91C86K) HEXYLENE GLYCOL (UNII: KEH0A3F75J) FERRIC OXIDE RED (UNII: 1K09F3G675) ZINC CHLORIDE (UNII: 86Q357L16B) GLYCERIN (UNII: PDC6A3C0OX) LYSINE (UNII: K3Z4F929H6) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59735-174-01 1 in 1 CARTON 02/01/2011 1 30 mL in 1 TUBE; 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 02/01/2011 Labeler - Mana Product, Inc (078870292) Registrant - Mana Product, Inc (078870292) Establishment Name Address ID/FEI Business Operations Mana Products,Inc 032870270 manufacture(59735-174) Establishment Name Address ID/FEI Business Operations Mana Products, Inc 078870292 manufacture(59735-174)