OPEN NATURE SPF 50 MINERAL SUNSCREEN- zinc oxide lotion 
SAFEWAY, 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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OPEN NATURE SPF 50 MINERAL SUNSCREEN LOTION

Active ingredient

Zinc Oxide 21.6%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use


When using this product

Stop use and ask a doctor if

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, C12-15 alkyl benzoate, caprylic/capric triglyceride, styrene/acrylates copolymer, octydodecyl citrate crosspolmyer, phenyl trimethicone, cetyl PEG/PPG-10/1 dimethicone, dimethicone, glycerin, polyhydroxystearic acid, ethyl methicone, cetyl dimethicone, silica, chrysanthemum parthenium (feverfew) flower/leaf/stem juice, glyceryl behenate, phenethyl alcohol, caprylyl glycol, bis-divinyl dimethicone/PEG-10 dimethicone crosspolymer, sodium chloride, phenoxyethanol, chlorphenesin

ON74629A1

OPEN NATURE SPF 50 MINERAL SUNSCREEN 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-723
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE216 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
GLYCERYL MONOBEHENATE (UNII: A626UU0W2A)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
GLYCERIN (UNII: PDC6A3C0OX)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TANACETUM PARTHENIUM FLOWER (UNII: 7TVV9D7I89)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
WATER (UNII: 059QF0KO0R)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21130-723-0389 mL in 1 TUBE; Type 0: Not a Combination Product12/05/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34612/05/2018
Labeler - SAFEWAY, INC. (009137209)

Revised: 1/2022
Document Id: d4f30568-37b5-2d92-e053-2a95a90a7ef8
Set id: a6020d2f-55c4-adfc-e053-2a95a90ad238
Version: 3
Effective Time: 20220106
 
SAFEWAY, INC.