NATIVE MINERAL FACE BROAD SPECTRUM SPF 30 COCONUT AND PINEAPPLE- zinc oxide lotion 
The Procter & Gamble Manufacturing Company

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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Native Mineral Face Lotion Broad Spectrum SPF 30 Coconut and Pineapple

Drug Facts

ZINC OXIDE 20%

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

Directions

Other information

Inactive ingredients

water, caprylic/capric triglyceride, coconut alkanes, glycerin, cetearyl alcohol, coco-glucoside, arachidyl alcohol, behenyl alcohol, arachidyl glucoside, polyhydroxystearic acid, benzyl alcohol, xanthan gum, coco-caprylate/caprate, fragrance, tocopherol, persea gratissima (avocado) oil, helianthus annuus (sunflower) seed oil

Distr. by Native San Francisco, CA 94111

Questions or comments?

Please contact support#\@nativecos.com

PRINCIPAL DISPLAY PANEL - 50 mL Tube

COCONUT & PINEAPPLE

NO OXYBENZONE

NO OCTINOXATE

NATIVE

MINERAL FACE LOTION

SUNSCREEN WITH ZINC OXIDE

BROAD SPECTRUM

SPF 30

1.7 FL OZ (50 mL)

Native

NATIVE MINERAL FACE BROAD SPECTRUM SPF 30 COCONUT AND PINEAPPLE 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-549
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE20 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
COCONUT ALKANES (UNII: 1E5KJY107T)  
COCO GLUCOSIDE (UNII: ICS790225B)  
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
AVOCADO OIL (UNII: 6VNO72PFC1)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
TOCOPHEROL (UNII: R0ZB2556P8)  
DOCOSANOL (UNII: 9G1OE216XY)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-549-5050 mL in 1 TUBE; Type 0: Not a Combination Product04/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35204/01/2021
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 7/2023
Document Id: ffd70a87-6fa9-2453-e053-6294a90adace
Set id: bdc063b6-62c4-17d5-e053-2a95a90ab8e4
Version: 3
Effective Time: 20230706
 
The Procter & Gamble Manufacturing Company