SOFTEN SURE FOAM ANTIMICROBIAL- chloroxylenol liquid

Soften Sure Foam Antimicrobial by

Drug Labeling and Warnings

Soften Sure Foam Antimicrobial by is a Otc medication manufactured, distributed, or labeled by Best Sanitizers, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Chloroxylenol 1.0%

Purpose

Antimicrobial Hand Cleanser

Uses

• Handwash to help reduce bacteria that potentially can cause diseases
• Helps to prevent cross contaminiation by hand contact
• Helps to prevent drying of the skin
• Recommended for repeated use
  

Warnings

• For external use only

When Using this product

• Do not use in or near eyes.

Keep out of reach of children

In case of accidental ingestion seek medical attention or contact a poison center immediately.

Directions

• Wet hands and forearms
• Apply an application to hands and forearms
• Scrub thoroughly for at least 30 seconds (include the fingernails and the cuticles)
• Rinse
  

Other Information

• Store in a cool dry place below 104° F

Inactive ingredients

purified water, potassium cocoate, tetrasodium EDTA, FDC No. 1, Yellow No.5, fragrance

Questions?

Contact Best Sanitizers Mon-Fri 9am - 4pm PST at 888-225-3267

PRINCIPAL DISPLAY PANEL

NDC: 59900-211-06

NDC: 59900-211-10

NDC: 59900-211-11

Soften Sure Foam Soap antimicrobial

INGREDIENTS AND APPEARANCE

SOFTEN SURE FOAM ANTIMICROBIAL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59900-211
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	10 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
EDETATE SODIUM (UNII: MP1J8420LU)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59900-211-06	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2008
2	NDC: 59900-211-10	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2008
3	NDC: 59900-211-11	1000 mL in 1 BAG; Type 0: Not a Combination Product	09/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/01/2008

Labeler - Best Sanitizers, Inc (957473614)

Establishment
Name	Address	ID/FEI	Business Operations
Best Sanitizers, Inc		627278224	manufacture(59900-211)