AVEENO POSITIVELY MINERAL SENSITIVE SKIN SUNSCREEN BROAD SPECTRUM SPF 50- 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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Aveeno Positively Mineral Sensitive Skin Sunscreen

Broad spectrum SPF 50

Drug Facts

Active ingredients

Zinc Oxide (21.6%)

Purpose

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, C12-15 Alkyl Benzoate, Dimethicone, Glycerin, Phenoxyethanol, Phenyl Trimethicone, Styrene/Acrylates copolymer, Octyl dodecyl Citrate Crosspolymer, Cetyl PEG/PPG-10/1 Dimethicone, Polyhydroxystearic acid, Silica, Ethyl methicone,Cetyl Dimethicone, Triethoxycaprylylsilane, Glyceryl Behenate, Sodium Chloride,Acrylates/Dimethicone copolymer, Chlorphenesin, Phenethyl alcohol, Avena Sativa (Oat) Kernel flour, Caprylyl Glycol,Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem juice

Questions?

886-428-3366; Outside US, dial collect 215-273-8755 www.aveeno.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

DERMATOLOGIST
 RECOMMENDED

Aveeno ®
POSITIVELY
MINERAL™

sensitive skin
sunscreen

BROAD SPECTRUM SPF 50

naturally-sourced
100% zinc oxide
active ingredient
sweat + water resistant
(80 min)

SPF

50

3.0 fl. oz (88 mL)

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label
AVEENO POSITIVELY MINERAL SENSITIVE SKIN SUNSCREEN BROAD SPECTRUM SPF 50 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0395
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
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
OATMEAL (UNII: 8PI54V663Y)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)  
FEVERFEW (UNII: Z64FK7P217)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0395-388 mL in 1 TUBE; Type 0: Not a Combination Product10/01/201811/27/2024
2NDC:69968-0395-114 mL in 1 TUBE; Type 0: Not a Combination Product10/01/201801/12/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/01/201811/27/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 5/2023
Document Id: fc7031f4-4d26-a376-e053-6394a90ab971
Set id: 5854a6e2-9854-423f-8ab8-d859143a289c
Version: 7
Effective Time: 20230524
 
Johnson & Johnson Consumer Inc.