PANOXYL- benzoyl peroxide cream 
Crown Laboratories

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Panoxyl Acne Wash

Active ingredient (4%)

Benzoyl peroxide 4%

Active ingredient (10%)

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 (4%)

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

Inactive ingredients (10%)

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, stearic acid, t-butyl alcohol, xanthan gum

Questions or comments?

call 1-833-279-6522

Panoxyl 4% Tube

NDC 0316-0227-06

DERMATOLOGIST RECOMMENDED

PanOxyl®

ACNE CREAMY WASH

4% Benzoyl Peroxide

Daily Control

Clears Existing Acne and Helps Prevent New Breakouts from Forming

Treats Acne on Face and Body

Formulated to be Gentle on Skin

Net wt. 6oz (170g)

TAMPER-EVIDENT FEATURE:

For your protection, do not use if foil seal on tube is broken or missing.

P11532.03

PANOXYL is a registered trademark of Crown Laboratories, Inc.

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

PanOxyl 4pct Wash Tube

Panoxyl 4% Carton

NDC 0316-0227-06

DERMATOLOGIST RECOMMENDED

PanOxyl®

ACNE CREAMY WASH

4% Benzoyl Peroxide

Daily Control

Clears Existing Acne and Helps Prevent New Breakouts from Forming

Treats Acne on Face and Body

Formulated to be Gentle on Skin

Net wt. 6oz (170g)

PANOXYL is a registered trademark of Crown Laboratories, Inc.

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

P11730.02

PanOxyl 4pct Wash Carton

Panoxyl 10% Tube

NDC 0316-0228-55

DERMATOLOGIST RECOMMENDED

PanOxyl®

ACNE FOAMING WASH

10% Benzoyl Peroxide

Maximum Strength

Clears Existing Acne and Helps Prevent New Breakouts from Forming

Treats Acne on Face and Body

Maximum Strength without a Prescription

Net wt. 5.5oz (156g)

TAMPER-EVIDENT FEATURE:

For your protection, do not use if foil seal on tube is broken or missing.

P11536.03

PANOXYL is a registered trademark of Crown Laboratories, Inc.

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

PanOxyl 10pct Wash Tube

Panoxyl 10% Carton

NDC 0316-0228-55

DERMATOLOGIST RECOMMENDED

PanOxyl ®

ACNE FOAMING WASH

10% Benzoyl Peroxide

Maximum Strength

Clears Existing Acne and Helps Prevent New Breakouts from Forming

Treats Acne on Face and Body

Maximum Strength without a Prescription

PANOXYL is a registered trademark of Crown Laboratories, Inc.

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

P11731.02

PanOxyl 10pct Wash Carton

PANOXYL 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0227
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE58.7 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)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
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)  
SORBITOL (UNII: 506T60A25R)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0227-061 in 1 CARTON12/01/2018
1170 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
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 PEROXIDE146.7 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
PALMITIC ACID (UNII: 2V16EO95H1)  
DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
XANTHAN GUM (UNII: TTV12P4NEE)  
WATER (UNII: 059QF0KO0R)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
PROPANEDIOL (UNII: 5965N8W85T)  
SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0228-551 in 1 CARTON12/01/2018
1156 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0316-0228-011 in 1 CARTON01/09/2023
228 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:0316-0228-0385 g in 1 TUBE; Type 0: Not a Combination Product02/26/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00603/25/2011
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories079035945manufacture(0316-0227, 0316-0228)

Revised: 11/2023
Document Id: 0a0b34ba-2f57-27a4-e063-6394a90a0777
Set id: 7b301b94-3cc8-b05b-e053-2991aa0aa561
Version: 20
Effective Time: 20231113
 
Crown Laboratories