FDA.reportPublic FDA data

Neutrogena MINERAL UV TINT FACE LIQUID SPF 30

Manufacturer
Acupac Packaging, Inc.
Effective date
2026-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:50

Label at a glance#

ProductNeutrogena MINERAL UV TINT FACE MEDIUM SPF 30
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure11 sections

Indications and 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

Dosage and administration

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 incl...

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 3.2%, Zinc Oxide 21.6%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

  • Do not useon damaged or broken skin

OTC - WHEN USING SECTION

  • When using this productkeep out of eyes .Rinse with water to remove.

OTC - STOP USE SECTION

  • Stop use and ask a doctor ifrash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

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 - 1.4 mL pouch Label - MEDIUM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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)

1.4 ml

Mineral UV Tint MediumMineral UV Tint Medium

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixJNJ7000A03Mineral UV Tint Medium.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52328-303-02Neutrogena MINERAL UV TINT FACE MEDIUM SPF 301.4 mL in 1 POUCHLOTION1.41
52328-303-02Neutrogena MINERAL UV TINT FACE MEDIUM SPF 3024 in 1 TRAYLOTION241

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52328-30352328-303-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOHEXADECANE918X1OUF1EIACT
DIMETHICONE92RU3N3Y1OIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)035JKJ76MTIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
XANTHAN GUMTTV12P4NEEIACT
FERRIC OXIDE RED1K09F3G675IACT
STEARIC ACID4ELV7Z65APIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
ISONONYL ISONONANOATES4V5BS6GCXIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Neutrogena MINERAL UV TINT FACE MEDIUM SPF 30TITANIUM DIOXIDE, ZINC OXIDEAcupac Packaging, Inc.4ef4d44e-3421-535f-e063-6294a90a2fea2026-04-08WarningsExact identifier
ndc (package): 52328-303-02
ndc (product): 52328-303
ndc11 (package): 52328030302
spl id: 4ef4dc4f-2492-3d4d-e063-6294a90ab74b
spl set id: 4ef4d44e-3421-535f-e063-6294a90a2fea

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.