NEUTROGENA MINERAL UV TINT FACE MEDIUM DEEP SPF 30- titanium dioxide, zinc oxide lotion NEUTROGENA MINERAL UV TINT FACE DEEP SPF 30- titanium dioxide, zinc oxide lotion NEUTROGENA MINERAL UV TINT FACE LIGHT SPF 30- titanium dioxide, zinc oxide lotion NEUTROGENA MINERAL UV TINT FACE MEDIUM SPF 30- titanium dioxide, zinc oxide lotion

Neutrogena MINERAL UV TINT FACE MEDIUM SPF 30 by

Drug Labeling and Warnings

Neutrogena MINERAL UV TINT FACE MEDIUM SPF 30 by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Titanium Dioxide 3.2%, Zinc Oxide 21.6%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other 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

• Shake well before use
• apply generously 15 minutes before sun exposure
• reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• 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
• children under 6 months of age: Ask a doctor

Other information

• protect this product from excessive heat and direct sun
• May stain some fabrics

Inactive ingredients

Water, Isohexadecane, Dicaprylyl Carbonate, Dimethicone, Isopropyl Palmitate, Isononyl Isononanoate, Cetyl PEG/PPG-10/1 Dimethicone, C12-15 Alkyl Benzoate, Sodium Chloride, Polyhydroxystearic Acid, Tocopheryl Acetate, Triethoxycaprylylsilane, Sorbitan Sesquioleate, Phenoxyethanol, Ethylhexylglycerin, Dimethiconol, Aluminum Hydroxide, Dimethicone Crosspolymer, Stearic Acid, Xanthan Gum, Iron Oxides

Questions?

Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com

SPL UNCLASSIFIED SECTION

Distributed by:
Kenvue Brands LLC

Summit, NJ 07901

PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - LIGHT

NEW

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

PURESCREEN+ TM

MINERAL

UV ● TINT

FACE LIQUID

with

Vitamin E

LIGHT

30

TINTED SUNSCREEN

BROAD SPECTRUM SPF 30

UVA/UVB PROTECTION

neutral undertone

for flexible coverage

water resistant (80 minutes)

1.1 FL OZ (32mL)

PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - DEEP

NEW

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

PURESCREEN+ TM

MINERAL

UV ● TINT

FACE LIQUID

with

Vitamin E

DEEP

30

TINTED SUNSCREEN

BROAD SPECTRUM SPF 30

UVA/UVB PROTECTION

neutral undertone

for flexible coverage

water resistant (80 minutes)

1.1 FL OZ (32mL)

PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - MEDIUM

NEW

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

PURESCREEN+ TM

MINERAL

UV ● TINT

FACE LIQUID

with

Vitamin E

MEDIUM

30

TINTED SUNSCREEN

BROAD SPECTRUM SPF 30

UVA/UVB PROTECTION

neutral undertone

for flexible coverage

water resistant (80 minutes)

1.1 FL OZ (32mL)

PRINCIPAL DISPLAY PANEL - 32 mL Carton Label - MEDIUM DEEP

NEW

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

PURESCREEN+ TM

MINERAL

UV ● TINT

FACE LIQUID

with

Vitamin E

MEDIUM

DEEP

30

TINTED SUNSCREEN

BROAD SPECTRUM SPF 30

UVA/UVB PROTECTION

neutral undertone

for flexible coverage

water resistant (80 minutes)

1.1 FL OZ (32mL)

INGREDIENTS AND APPEARANCE

NEUTROGENA MINERAL UV TINT FACE MEDIUM DEEP SPF 30 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0784
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	216 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	32 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
XANTHAN GUM (UNII: TTV12P4NEE)
FERRIC OXIDE RED (UNII: 1K09F3G675)
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0784-1	1 in 1 CARTON	12/05/2022
1		32 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69968-0784-2	24 in 1 TRAY	03/04/2024
2		1.4 mL in 1 POUCH; 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	12/05/2022

NEUTROGENA MINERAL UV TINT FACE DEEP SPF 30 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0783
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	216 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	32 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
XANTHAN GUM (UNII: TTV12P4NEE)
FERRIC OXIDE RED (UNII: 1K09F3G675)
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0783-1	1 in 1 CARTON	12/05/2022
1		32 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69968-0783-2	24 in 1 TRAY	03/04/2024
2		1.4 mL in 1 POUCH; 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	12/05/2022

NEUTROGENA MINERAL UV TINT FACE LIGHT SPF 30 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0781
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	32 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	216 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
XANTHAN GUM (UNII: TTV12P4NEE)
FERRIC OXIDE RED (UNII: 1K09F3G675)
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0781-1	1 in 1 CARTON	12/05/2022
1		32 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69968-0781-2	24 in 1 TRAY	03/04/2024
2		1.4 mL in 1 POUCH; 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	12/05/2022

NEUTROGENA MINERAL UV TINT FACE MEDIUM SPF 30 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0782
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	216 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	32 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOHEXADECANE (UNII: 918X1OUF1E)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
XANTHAN GUM (UNII: TTV12P4NEE)
FERRIC OXIDE RED (UNII: 1K09F3G675)
STEARIC ACID (UNII: 4ELV7Z65AP)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0782-1	1 in 1 CARTON	12/05/2022
1		32 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 69968-0782-2	24 in 1 TRAY	03/04/2024
2		1.4 mL in 1 POUCH; 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	12/05/2022

Labeler - Kenvue Brands LLC (118772437)