NEUTROGENA ULTRA SHEER BODY MIST SUNSCREEN BROAD SPECTRUM SPF 70- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone aerosol, spray 
Johnson & Johnson Consumer Inc.

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Neutrogena ® Ultra Sheer ® BODY MIST SUNSCREEN Broad Spectrum SPF 70

Drug Facts

Active ingredientsPurpose
Avobenzone (3%)Sunscreen
Homosalate (15%)Sunscreen
Octisalate (5%)Sunscreen
Octocrylene (4%)Sunscreen
Oxybenzone (6%)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.
    • keep away from face to avoid breathing it

  • 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.

  • Danger: Flammable. Contents under pressure. Do not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperature below 120°F (48°C). Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Directions

Other information

Inactive ingredients

Alcohol Denat., Isobutane, Butyloctyl Salicylate, Acrylates/ Octylacrylamide Copolymer, Diethylhexyl 2,6 – Naphthalate, Fragrance, Tocopheryl Acetate, Ascorbyl Palmitate, Retinyl Palmitate, Tocopherol

Questions or Comments?

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

PRINCIPAL DISPLAY PANEL - 141 g Can Label

Neutrogena ®
#1 DERMATOLOGIST RECOMMENDED BRAND

Ultra sheer ®
body mist
sunscreen

BROAD SPECTRUM SPF 70

70

helioplex ®
broad spectrum uva•uvb

weightless clean feel
non-greasy
water resistant (80 minutes)

NET WT 5.0 OZ (141 g)

Principal Display Panel - 141 g Can Label
NEUTROGENA ULTRA SHEER BODY MIST  SUNSCREEN BROAD SPECTRUM SPF 70
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0171
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE150 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE40 mg  in 1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
ISOBUTANE (UNII: BXR49TP611)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
TOCOPHEROL (UNII: R0ZB2556P8)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0171-5141 g in 1 CAN; Type 0: Not a Combination Product10/05/2007
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/05/2007
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 10/2023
Document Id: 07d4da22-2ce9-4755-e063-6294a90a5bdf
Set id: 6c578ef8-5648-4428-b9a2-0952f9625253
Version: 8
Effective Time: 20231016
 
Johnson & Johnson Consumer Inc.