Neutrogena Healthy Skin Face Lotion with Sunscreen SPF 15

Neutrogena Healthy Skin Face by

Drug Labeling and Warnings

Neutrogena Healthy Skin Face by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA HEALTHY SKIN FACE  SUNSCREEN SPF 15- octinoxate and oxybenzone 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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Neutrogena Healthy Skin Face Lotion with Sunscreen SPF 15

Drug Facts

Active ingredients

Octinoxate 7.5%
Oxybenzone 5 %

Purpose

Sunscreen

Use

  • Helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert

Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

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

For Sunscreen Use

  • apply liberally 15 minutes before sun exposure
  • use a water resistant sunscreen if swimming or sweating
  • reapply at least every 2 hours
  • Children under 6 months of age: Ask a doctor

Other information

  • Protect this product from excessive heat and direct sun
  • You may experience some irritation while using this product. This is normal and temporary. If irritation persists, use once a day, every other day, until your skin adjusts, then revert to daily use.
  • Sunburn Alert: This prouct contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Limit sun exposure while using this product and use a sunscreen for a week after use.

Inactive Ingredients

Water, Glycolic Acid, C12-15 Alkyl Benzoate, Dicaprylyl Maleate, Sodium Glycolate, Cetyl Alcohol, Glycerin, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Tocopheryl Acetate, Retinyl Palmitate, Ascorbic Acid Polypeptide, Panthenol, Bisabolol, Tetrasodium EDTA, Xanthan Gum, Methylparaben, Propylparaben, Diazolidinyl Urea, Fragrance

Questions or Comments?

visit www.neutrogenamena.com. Call toll-free 800-582-4048 or 215-273-8755 (collect)

Dist. by Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton

see new information

NEUTROGENA
Healthy Skin®
face lotion

with
sunscreen

SPF 15

A Moisturizer with Multi-Vitamins
and Alpha-Hydroxy

  • Softens and smoothes rough,
    uneven skin while reducing
    the look of fine lines

Neutrogena®

DERMATOLOGIST
RECOMMENDED

2.5 FL OZ (73mL)

Principal Display Panel - 73 mL Bottle Carton
NEUTROGENA HEALTHY SKIN FACE   SUNSCREEN SPF 15
octinoxate and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 10812-934
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate75 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycolic Acid (UNII: 0WT12SX38S)  
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
Dioctyl Maleate (UNII: OD88G8439L)  
Sodium Glycolate (UNII: B75E535IMI)  
Cetyl Alcohol (UNII: 936JST6JCN)  
Glycerin (UNII: PDC6A3C0OX)  
Stearic Acid (UNII: 4ELV7Z65AP)  
Glyceryl Monostearate (UNII: 230OU9XXE4)  
PEG-100 Stearate (UNII: YD01N1999R)  
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
Vitamin A Palmitate (UNII: 1D1K0N0VVC)  
Panthenol (UNII: WV9CM0O67Z)  
Levomenol (UNII: 24WE03BX2T)  
Edetate Sodium (UNII: MP1J8420LU)  
Xanthan Gum (UNII: TTV12P4NEE)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Diazolidinyl Urea (UNII: H5RIZ3MPW4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 10812-934-021 in 1 CARTON11/01/201209/24/2016
173 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35211/01/201209/24/2016
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 3/2020
Document Id: 3aacbd96-2fd1-4729-bf93-2eb17c1dd8f6
Set id: e579764c-ddd2-4026-a351-69cde629c247
Version: 5
Effective Time: 20200323