SULFO LO- sulfur 3% soap bar soap 
Crown Laboratories

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Sulfo-Lo Cleansing Bar Soap

Active ingredients

Sulfur 3%

Purpose

Acne Treatment

Uses

Deep cleansing antibacterial soap for management of acne, blackheads and comedones.

Warnings

For external use only • Avoid contact with eyes, wash with water if exposed

•Do no use on

• broken skin • large areas of skin

• When using this product

• apply only to areas with acne • 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 • If undue irritation persists consult a physician

• Keep out of reach of children.

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

Directions

• Work into a lather and rinse with warm water • Use daily as skin cleanser or as directed by a physician.

Other information

Store at 20˚-25˚C (68˚-77˚F) [see USP Controlled Room Temperature].

Inactive ingredients

Sodium Tallowate, Sodium Cocoate/Sodium Palm Kernelate, Water (Aqua), Glycerin, Fragrance (Parfum), Sodium Chloride, Butyrospermum parkii (Shea) Butter, Yellow 5 (CI19140), Titanium Dioxide (CI77891), Pentasodium Pentetate, Tetrasodium Etidronate, Iron Oxides (CI77492), Tocopheryl Acetate

NDC 0316-0118-35

sulfo lo®

Cleansing Bar Soap

Helps Treat and Manage Acne, Blackheads and Comedones

DERMATOLOGIST RECOMMENDED

Net wt. 3.5oz (99 grams)

Distributed by: Crown Laboratories, Inc., Johnson City, TN 37604
www.crownlaboratories.com | 800.334.4286 | Made in the USA

P9100.06

P910006

SULFO LO 
sulfur 3% soap bar soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-0118
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR30 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
SODIUM TALLOWATE, BEEF (UNII: 07RIK6QMEW)  
SODIUM COCOATE (UNII: R1TQH25F4I)  
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)  
ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)  
BROWN IRON OXIDE (UNII: 1N032N7MFO)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SHEA BUTTER (UNII: K49155WL9Y)  
BASIC YELLOW 5 (UNII: 07BP340B4T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-0118-3599 g in 1 CARTON; Type 0: Not a Combination Product11/01/1965
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00611/01/1965
Labeler - Crown Laboratories (079035945)
Registrant - Crown Laboratories (079035945)

Revised: 11/2023
Document Id: 0aacd913-975c-b6f8-e063-6294a90a5f3e
Set id: 89577417-76a0-cb04-e053-2995a90a5733
Version: 4
Effective Time: 20231121
 
Crown Laboratories