NEUTROGENA COMPLETE ACNE THERAPY SOLUTION- salicylic acid, avobenzone, octisalate, octocrylene, oxybenzone, and benzoyl peroxide 
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® Complete Acne Therapy Solution

Neutrogena® SKIN POLISHING ACNE CLEANSER

Drug Facts

Active ingredient

Salicylic Acid 0.5%

Purpose

Acne treatment

Use

  • For the treatment of acne

Warnings

For external use only

  • When using this product
    • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
    • avoid contact with eyes. If contact occurs, flush thoroughly with water.

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • wet face. Squeeze into hands
  • apply to face and massage gently
  • rinse thoroughly
  • if excessive drying of peeling occurs, reduce application to every other day

Other information

Sunburn Alert: This product contains an alpha hydroxy acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards.

Store at room temperature.

Inactive ingredients

Water, Sodium Methyl Cocoyl Taurate, Cocamidopropyl Betaine, Sodium Cocoamphoacetate, Sodium Chloride, Glycol Distearate, Polyethylene, Glycolic Acid, Sodium Lactate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Polyquaternium-11, Disodium EDTA, Fragrance, Citric Acid, Sodium Hydroxide

Questions?

Visit www.neutrogena.com or call toll-free 800-582-4048 or 215-273-8755 (collect)

Neutrogena® OIL-FREE MOISTURE Broad Spectrum SPF 15

Drug Facts

Active ingredients

Avobenzone (1.5%), Octisalate (5%), Octocrylene (3%), Oxybenzone (4%)

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

For Sunscreen Use

  • apply liberally and evenly 15 minutes before sun exposure
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating

    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 of age: Ask a doctor

Other information

  • protect this product from excessive heat and direct sun
  • may stain some fabrics

Inactive ingredients

Water, Octyldodecyl Neopentanoate, Glycerin, Emulsifying Wax NF, Glyceryl Stearate, PEG-100 Stearate, Dimethicone, Phenoxyethanol, Ethylhexylglycerin, Caprylyl Glycol, Carbomer, Triethanolamine, Methylparaben, Disodium EDTA, Ethylene Brassylate, Dipropylene Glycol, Dimethyl Heptenal

Questions?

Visit www.neutrogena.com or call toll-free 800-582-4048 or 215-273-8755 (collect)

Neutrogena® ACNE CONTROL LOTION

Drug Facts

Active ingredient

Benzoyl Peroxide 2.5%

Purpose

Acne Medication

Use

  • For the treatment of acne

Warnings

For external use only

  • When using this product
    • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Do not use if you

  • have very sensitive skin.
  • are sensitive to benzoyl peroxide.

When using this product

  • avoid unnecessary sun exposure and use a sunscreen.
  • avoid contact with the eyes, lips, and mouth.
  • avoid contact with hair or dyed fabrics, which may be bleached by this product.
  • skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask a doctor if

  • irritation becomes severe.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • clean the skin thoroughly before applying this product.
  • cover the entire affected area with a thin layer one to three times daily.
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
  • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Inactive ingredients

Water, Carbomer Homopolymer type B, Ethylhexylglycerin, Sodium Hydroxide, Chlorphenesin, Disodium EDTA, Laureth-4, Hydroxypropyl Methylcellulose

Questions?

Visit www.neutrogena.com or call toll-free 800-582-4048 or 215-273-8755 (collect)

Dist by: ®T.M.(M.R.)©Neutrogena Corporation Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - Kit Carton

NEW FORMULA

approximately 2 months supply

CLINICALLY
PROVEN
overnight results
with acne
control lotion

complete acne therapy
solution

Reduces size and redness overnight without over-drying skin
Controls breakouts with 2 dermatologist recommended medicines

Neutrogena®

oil-free moisture with sunscreen
Broad Spectrum SPF 15
1.7 L. OZ. (50mL)
acne control lotion with
benzoyl peroxide acne medicine
1.4 FL. OZ. (40mL)
skin polishing acne cleanser
with salicylic acid acne treatment
5.1 FL.OZ. (150mL)
PRINCIPAL DISPLAY PANEL - Kit Carton
NEUTROGENA COMPLETE ACNE THERAPY SOLUTION 
salicylic acid, avobenzone, octisalate, octocrylene, oxybenzone, and benzoyl peroxide kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-995
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-995-991 in 1 CARTON11/01/201511/01/2018
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 150 mL
Part 21 TUBE 50 mL
Part 31 TUBE 40 mL
Part 1 of 3
NEUTROGENA SKIN POLISHING ACNE CLEANSER 
salicylic acid gel
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Sodium Methyl Cocoyl Taurate (UNII: JVL98CG53G)  
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
Sodium Cocoamphoacetate (UNII: W7Q5E87674)  
Sodium Chloride (UNII: 451W47IQ8X)  
Glycol Distearate (UNII: 13W7MDN21W)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Glycolic Acid (UNII: 0WT12SX38S)  
Sodium Lactate (UNII: TU7HW0W0QT)  
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate (UNII: H2KVQ74JM4)  
Edetate Disodium (UNII: 7FLD91C86K)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/14/2014
Part 2 of 3
NEUTROGENA OIL FREE BROAD SPECTRUM SPF15 
avobenzone, octisalate, octocrylene, and oxybenzone lotion
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone15 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene30 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Octyldodecyl Neopentanoate (UNII: X8725R883T)  
Glycerin (UNII: PDC6A3C0OX)  
Glyceryl Monostearate (UNII: 230OU9XXE4)  
PEG-100 Stearate (UNII: YD01N1999R)  
Dimethicone (UNII: 92RU3N3Y1O)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Caprylyl Glycol (UNII: 00YIU5438U)  
Trolamine (UNII: 9O3K93S3TK)  
Methylparaben (UNII: A2I8C7HI9T)  
Edetate Disodium (UNII: 7FLD91C86K)  
Ethylene Brassylate (UNII: 9A87HC7ROD)  
Dipropylene Glycol (UNII: E107L85C40)  
2,6-Dimethyl-5-Heptenal (UNII: Z331YX9EL9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/15/2014
Part 3 of 3
NEUTROGENA ACNE CONTROL 
benzoyl peroxide lotion
Product Information
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Chlorphenesin (UNII: I670DAL4SZ)  
Edetate Disodium (UNII: 7FLD91C86K)  
Laureth-4 (UNII: 6HQ855798J)  
Hypromelloses (UNII: 3NXW29V3WO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
140 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/14/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D11/01/201511/01/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2016
 
Johnson & Johnson Consumer Inc.