Label: DOLCE AND GABBANA BLUEBERRY NUTRI TINT SPF 20 10N LIGHT MEDIUM TESTER- zinc oxide emulsion
- NDC Code(s): 84003-054-01, 84003-054-02
- Packager: Dolce & Gabbana Beauty S.R.L
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 26, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
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Directions
- Apply generously 15 minutes before sun exposure
- Reapply at least every 2 hours
- Use a water resistant sunscreen if swimming or sweating
- 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 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
- Children under 6 months of age: ask a doctor
SHAKE WELL BEFORE USE
- Other information
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Inactive ingredients
WATER/EAU (AQUA), DIMETHICONE, C12-15 ALKYL BENZOATE, PHENYL TRIMETHICONE, TALC, PEG-10 DIMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, TRIMETHYLSILOXYSILICATE, GLYCERIN, ISOSTEARYL NEOPENTANOATE, GLYCERYL GLUCOSIDE, BIS-PEG/PPG-14/14 DIMETHICONE, ISODODECANE, PHENOXYETHANOL, SODIUM CHLORIDE, MICA, MAGNESIUM SULFATE, MENTHOXYPROPANEDIOL, SODIUM DEHYDROACETATE, HYDROGEN DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, BENZOIC ACID, C24-28 ALKYL METHICONE, DISTEARDIMONIUM HECTORITE, SILICA, ALUMINUM HYDROXIDE, DEHYDROACETIC ACID, VACCINIUM MYRTILLUS FRUIT EXTRACT, PROPYLENE CARBONATE, ETHYLHEXYLGLYCERIN, LAURETH-4, POTASSIUM SORBATE, SODIUM BENZOATE, LACTIC ACID, PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE: +/- MAY CONTAIN: TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499)
- Package Labelling: 84003-054-01
- Package Labelling: 84003-054-02
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INGREDIENTS AND APPEARANCE
DOLCE AND GABBANA BLUEBERRY NUTRI TINT SPF 20 10N LIGHT MEDIUM TESTER
zinc oxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84003-054 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 67 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) TALC (UNII: 7SEV7J4R1U) GLYCERIN (UNII: PDC6A3C0OX) ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q) GLYCERYL GLUCOSIDE (UNII: 3297VXM8Z6) BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE) ISODODECANE (UNII: A8289P68Y2) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) MICA (UNII: V8A1AW0880) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) 3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) BENZOIC ACID (UNII: 8SKN0B0MIM) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) DEHYDROACETIC ACID (UNII: 2KAG279R6R) BILBERRY (UNII: 9P2U39H18W) PROPYLENE CARBONATE (UNII: 8D08K3S51E) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LAURETH-4 (UNII: 6HQ855798J) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) LACTIC ACID (UNII: 33X04XA5AT) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84003-054-01 1 in 1 BOX 01/01/2025 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:84003-054-02 1 in 1 BOX 01/01/2025 2 30 mL in 1 BOTTLE; 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 01/01/2025 Labeler - Dolce & Gabbana Beauty S.R.L (442254105)
