PANOXYL- benzoyl peroxide cream 
Crown Laboratories

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Panoxyl Acne Foaming Wash

Active ingredient

Benzoyl peroxide 10%

Purpose

Acne medication

Use

Warnings

For external use only

Do not use if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

carbomer homopolymer type C, carbomer interpolymer type A, decyl glucoside, dimethicone, dioctyl sodium sulfosuccinate, glycerin, palmitic acid, polyacrylate crosspolymer-6, polyoxyl 40 stearate, propanediol, purified water, silica, sodium chloride, sodium citrate, sodium hydroxide, sodium laurylglucosides hydroxypropylsulfonate, sorbitan stearate, sorbitol, stearic acid, t-butyl alcohol, xanthan gum

Questions or comments?

call 1-833-279-6522

Panoxyl 10% Tube

PanOxyl®

ACNE FOAMING WASH

for Face & Body

10% Benzoyl Peroxide

Acne Treatment Wash

Maximum Strength

Clears existing acne and helps prevent new breakouts

Net wt. 5.5oz (156g)

DERMATOLOGIST RECOMMENDED

Distributed by: Crown Laboratories, Inc. Johnson City, TN 37604

P11536.04

P11536.04 Tube

Panoxyl 10% Carton

PanOxyl®

ACNE FOAMING WASH

for Face & Body

10% Benzoyl Peroxide

Acne Treatment Wash

Maximum Strength

Clears existing acne and helps prevent new breakouts

Maximum strength without a prescription

No.1 DERMATOLOGIST RECOMMENDED BENZOYL PEROXIDE BRAND

Net wt. 5.5oz (156g)

P11731.05

10pct carton

PANOXYL 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0228
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
XANTHAN GUM (UNII: TTV12P4NEE)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
PALMITIC ACID (UNII: 2V16EO95H1)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
PROPANEDIOL (UNII: 5965N8W85T)  
SODIUM LAURYLGLUCOSIDES HYDROXYPROPYLSULFONATE (UNII: Z6GFR7R72Y)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0228-011 in 1 CARTON10/12/2022
128 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0316-0228-0385 g in 1 TUBE; Type 0: Not a Combination Product11/12/2022
3NDC:0316-0228-551 in 1 CARTON12/01/2018
3156 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00603/25/2011
Labeler - Crown Laboratories (119508400)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories119508400manufacture(0316-0228)

Revised: 1/2026
Document Id: 48342795-9bf1-4541-e063-6394a90a10be
Set id: 1660f219-e789-91f1-e063-6294a90a7664
Version: 4
Effective Time: 20260112
 
Crown Laboratories