Neutrogena Sheer Zinc Mineral Sunscreen Stick Broad Spectrum SPF 50+

Neutrogena Sheer Zinc Mineral Sunscreen Stick Broad Spectrum SPF 50+

Drug Labeling and Warnings

Drug Details

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NEUTROGENA SHEER ZINC MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 PLUS- zinc oxide stick 
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 Sheer Zinc Mineral Sunscreen Stick Broad Spectrum SPF 50+

Drug Facts

Active ingredients

Zinc Oxide (21.6%)

Purpose

Sunscreen

Uses

  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

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

  • apply generously and evenly 15 minutes before sun exposure
  • ensure complete coverage to the area above the lip, nose, and tops of ears
  • reapply:
    • after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10 a.m. – 2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses
  • children under 6 months of age: Ask a doctor

Other information

  • protect this product from excessive heat and direct sun
  • may stain some fabrics
  • package contains small parts, which could cause a choking hazard

Inactive ingredients

Octyldodecyl Neopentanoate, C12-15 Alkyl Benzoate, Polyethylene, Paraffin, Silica, Neopentyl Glycol Diethylhexanoate, Ozokerite, Isopropyl Myristate, Adipic Acid/Diglycol Crosspolymer, Triethoxycaprylylsilane, Neopentyl Glycol Diisostearate, Caprylyl Glycol, Tocopheryl Acetate

Questions?

800-582-4048; Outside US, dial collect 215-273-8755.
neutrogena.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 42 g Canister Label

Neutrogena®

#1 DERMATOLOGIST RECOMMENDED BRAND

Sheer Zinc
mineral
sunscreen stick
BROAD SPECTRUM SPF 50+

50+
NEW
WITH VITAMIN E

water resistant (80 minutes)

NET WT 1.5 OZ (42g)

PRINCIPAL DISPLAY PANEL - 42 g Canister Label
NEUTROGENA SHEER ZINC MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 PLUS 
zinc oxide stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69968-0546
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide216 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Octyldodecyl Neopentanoate (UNII: X8725R883T)  
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Paraffin (UNII: I9O0E3H2ZE)  
Silicon Dioxide (UNII: ETJ7Z6XBU4)  
Neopentyl Glycol Diethylhexanoate (UNII: U68ZV6W62C)  
Ceresin (UNII: Q1LS2UJO3A)  
Isopropyl Myristate (UNII: 0RE8K4LNJS)  
ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19)  
Triethoxycaprylylsilane (UNII: LDC331P08E)  
Neopentyl Glycol Diisostearate (UNII: 4M6OQ34JWW)  
Caprylyl Glycol (UNII: 00YIU5438U)  
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69968-0546-142 g in 1 CANISTER; Type 0: Not a Combination Product10/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35210/01/2019
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 8/2019
 
Johnson & Johnson Consumer Inc.


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