Neutrogena® Clear Pore Daily Scrub

Neutrogena Clear Pore Daily Scrub by

Drug Labeling and Warnings

Neutrogena Clear Pore Daily Scrub by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA CLEAR PORE DAILY SCRUB- benzoyl peroxide suspension 
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® Clear Pore Daily Scrub

Drug Facts

Active ingredient

Benzoyl Peroxide 3.7%

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 this medication if you

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

When using this product

  • avoid unnecessary sun exposure and use sunscreen.
  • avoid contact with the eyes, lips, and mouth.
  • avoid contact with hair and dyed products, 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

Wet Face. Squeeze into hands. Apply to face and massage gently. Rinse thoroughly.

  • If going outside, apply sunscreen after using the product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Inactive ingredients

Water, Glycerin, Kaolin, Bentonite, Sodium Methyl Cocoyl Taurate, Titanium Dioxide, Polyethylene, Xanthan Gum, Citric Acid, Sodium Citrate, Trideceth-9, Disodium EDTA, Fragrance, PEG-5 Ethylhexanoate, Menthol.

Questions?

Call toll-free 800-582-4084 or 215-273-8755 (collect) www.neutrogena.com

  • Avoid storage at extreme temperatures (below 40°F and above 100°F).

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label

Clear
Pore
Daily Scrub

Benzoyl Peroxide formula
penetrates pores to clear
breakout causing impurities

Neutrogena®
benzoyl peroxide acne medication
4.2 FL OZ (125mL)

PRINCIPAL DISPLAY PANEL - 125 mL Tube Label
NEUTROGENA CLEAR PORE DAILY SCRUB 
benzoyl peroxide suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69968-0027
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide37 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Glycerin (UNII: PDC6A3C0OX)  
Kaolin (UNII: 24H4NWX5CO)  
Bentonite (UNII: A3N5ZCN45C)  
Sodium Methyl Cocoyl Taurate (UNII: JVL98CG53G)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
High Density Polyethylene (UNII: UG00KM4WR7)  
Xanthan Gum (UNII: TTV12P4NEE)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
Trideceth-9 (UNII: X9HD79I514)  
Edetate Disodium (UNII: 7FLD91C86K)  
PEG-5 Ethylhexanoate (UNII: OU427Y958F)  
Menthol, Unspecified Form (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69968-0027-4125 mL in 1 TUBE; Type 0: Not a Combination Product12/07/201512/29/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D12/07/201512/29/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2019
Document Id: 3b41b677-1f75-4f39-9c56-dd83a0f180bc
Set id: fba9fb4d-b879-430e-b552-12bb253e0594
Version: 2
Effective Time: 20191219
 
Johnson & Johnson Consumer Inc.