DOLCE AND GABBANA BLUEBERRY NUTRI TINT SPF 20 15N LIGHT MEDIUM TESTER- zinc oxide emulsion

Dolce and Gabbana Blueberry Nutri Tint SPF 20 15N Light Medium Tester by

Drug Labeling and Warnings

Dolce and Gabbana Blueberry Nutri Tint SPF 20 15N Light Medium Tester by is a Otc medication manufactured, distributed, or labeled by Dolce & Gabbana Beauty S.R.L. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Zinc Oxide 6.7%

Purpose

Sunscreen

Uses

• Helps prevent sunburn
• If uses directed with others sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

rash occurs.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

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

Protect the product in this container from excessive heat and direct sun.

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: 84003-057-01

Package Labelling: 84003-057-02

INGREDIENTS AND APPEARANCE

DOLCE AND GABBANA BLUEBERRY NUTRI TINT SPF 20 15N LIGHT MEDIUM TESTER 
zinc oxide emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84003-057
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: 84003-057-01	1 in 1 BOX	01/01/2025
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 84003-057-02	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)