NEUTROGENA MINERAL BEACH DEFENSE ACTIVE PERFORMANCE SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide, zinc oxide lotion 
Johnson & Johnson Consumer Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neutrogena Mineral Beach Defense Active Performance Sunscreen Broad Spectrum SPF 30

Drug Facts

Active ingredientsPurpose
Titanium Dioxide (6.5%), Zinc Oxide (18.7%)Sunscreen

Uses

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

Other information

Inactive ingredients

Water, Isohexadecane, C12-15 Alkyl Benzoate, Ethylhexyl methoxycrylene, Behenyl Alcohol, Steareth-21, Glyceryl Stearate, PEG-100 Stearate, Calcium Aluminum Borosilicate, Euphorbia Cerifera (Candelilla) Wax, Polyhydroxystearic Acid, Cetyl Alcohol, Triethoxycaprylylsilane, Aluminum Hydroxide, Xanthan Gum, Stearic Acid, Phenoxyethanol, Ethylhexylglycerin, Chlorphenesin, Tocopheryl Acetate, Disodium EDTA, Fragrance, Glycerin, Aloe Barbadensis Leaf Extract

Questions?

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

Distributed by:

JOHNSON & JOHNSON

CONSUMER INC.


Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 88 mL Tube

NEW

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

PURESCREEN+ TM

MINERAL

BEACH

DEFENSE ®

ACTIVE PERFORMANCE

BODY LOTION

30

SUNSCREEN

BROAD SPECTRUM SPF 30

UVA/UVB PROTECTION

100% mineral actives + aloe

water + sun ● water resistant (80 minutes)

3.0 FL OZ (88 mL)

Neutrogena_01

NEUTROGENA MINERAL BEACH DEFENSE ACTIVE PERFORMANCE SUNSCREEN BROAD SPECTRUM SPF 30 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0773
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE65 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE187 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
DOCOSANOL (UNII: 9G1OE216XY)  
STEARETH-21 (UNII: 53J3F32P58)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CANDELILLA WAX (UNII: WL0328HX19)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)  
XANTHAN GUM (UNII: TTV12P4NEE)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0773-388 mL in 1 TUBE; Type 0: Not a Combination Product10/04/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/04/2022
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ef4b305a-80f6-ceaf-e053-2a95a90a1ad3
Set id: e4af6288-89e6-3fb8-e053-2a95a90a12e0
Version: 2
Effective Time: 20230116
 
Johnson & Johnson Consumer Inc.