Neutrogena Wet Skin Swim Humidity Sweat Sunscreen Broad Spectrum SFP45 Plus

Dosage form: lotion
Ingredients: Avobenzone 30mg in 1mL, Homosalate 40mg in 1mL, Octisalate 50mg in 1mL, Octocrylene 40mg in 1mL, Oxybenzone 50mg in 1mL
Labeler: Neutrogena Corporation
NDC Code: 10812-525

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.

Neutrogena Wet Skin
Swim • Humidity • Sweat
Sunscreen Broad Spectrum SPF 45+

Drug Facts

Active ingredients

Avobenzone 3%
Homosalate 4%
Octisalate 5%
Octocrylene 4%
Oxybenzone 5%

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 15 minutes before sun exposure
  • 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 value of SPF 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 age: Ask a doctor

Other information
  • Protect this product from excessive heat and direct sun
  • May stain some fabrics

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Acrylates/Dimethicone Copolymer, Beeswax, Benzyl Alcohol, BHT, Caprylyl Glycol, Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, Chlorphenesin, Diethylhexyl 2,6-Naphthalate, Dimethicone, Dipotassium Glycyrrhizate, Disodium EDTA, Ethyl Methicone, Ethylhexylglycerin, Fragrance, Glyceryl Behenate, Glyceryl Dibehenate, Glyceryl Stearate, Nelumbo Nucifera Flower Wax, Octyldodecyl Citrate Crosspolymer, Oryza Sativa (Rice) Starch, PEG-100 Stearate, Phenoxyethanol, Silica, Tribehenin, Triethanolamine, Water

Questions or comments?

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

Dist. by Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 88mL Bottle Label

NEW

Neutrogena®

Wet skin

SWIM•HUMIDITY•SWEAT

SUNSCREEN

Broad
Spectrum
SPF45+

helioplex®
broad spectrum uva•uvb

full strength protection
on wet or dry skin
water resistant (80 minutes)

#1 DERMATOLOGIST
RECOMMENDED SUNCARE

3.0 FL OZ (88 mL)

NEUTROGENA WET SKIN SWIM HUMIDITY SWEAT   SUNSCREEN BROAD SPECTRUM SFP45 PLUS
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-525
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (Avobenzone) Avobenzone30 mg  in 1 mL
Homosalate (Homosalate) Homosalate40 mg  in 1 mL
Octisalate (Octisalate) Octisalate50 mg  in 1 mL
Octocrylene (Octocrylene) Octocrylene40 mg  in 1 mL
Oxybenzone (Oxybenzone) Oxybenzone50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Yellow Wax 
Benzyl Alcohol 
Butylated Hydroxytoluene 
Caprylyl Glycol 
Chlorphenesin 
Diethylhexyl 2,6-Naphthalate 
Dimethicone 
Glycyrrhizinate Dipotassium 
Edetate Disodium 
Ethylhexylglycerin 
Glyceryl Dibehenate 
Glyceryl Monostearate 
Nelumbo Nucifera Flower Wax 
Starch, Rice 
PEG-100 Stearate 
Phenoxyethanol 
Silicon Dioxide 
Tribehenin 
Trolamine 
Water 
Packaging
#Item CodePackage Description
1NDC:10812-525-0188 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35209/19/2012
Labeler - Neutrogena Corporation (008254617)
Registrant - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

Revised: 09/2012
 
Neutrogena Corporation

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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