ALPET E2 SANITIZING FOAM- chloroxylenol soap

Alpet E2 Sanitizing Foam by

Drug Labeling and Warnings

Alpet E2 Sanitizing Foam by is a Otc medication manufactured, distributed, or labeled by Best Sanitizer, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Chloroxylenol 1.5% w/w            

Purpose

Antiseptic Hand Cleanser

Uses

• Helps reduce bacteria that potentially can cause diseases
• Helps to prevent cross contamination by hand contact
  

Warnings

• For external use only

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.
In case of eye contact, flush with water for 15 minutes, if irritation persists, get medical attention.
In case of accidental ingestion, seek medical attention or contact a poison control center immediately.
This product must be dispensed from an adequate dispenser located a sufficient distance from processing line to prevent accidental product contamination.
Do not contaminate water, food or feed by storage and disposal.

Directions

• Apply cleaner to palm of hand
• Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 30 seconds
• Rinse with water until all cleaner is removed from hands
• Dry completely (incomplete drying may lead to happed skin)
  

Other information

• Store in a cool dry place below 104° F
  

Inactive ingredients

Water, Sodium Laureth Sulfate, Isopropyl alcohol, Phenoxyethanol, Glycerine, Triclosan, TetraSodium EDTA, Citric Acid

Questions?

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

PRINCIPAL DISPLAY PANEL

NDC: 59900-208-01

NDC: 59900-208-02

NDC: 59900-208-03

NDC: 59900-208-04

NDC: 59900-208-05

NDC: 59900-208-06

NDC: 59900-208-07

NDC: 59900-208-08

NDC: 59900-208-09

Alpet E2 Sanitizing Foam Soap

For Food Industry Professionals

INGREDIENTS AND APPEARANCE

ALPET E2 SANITIZING FOAM 
chloroxylenol soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59900-208
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	15 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
TRICLOSAN (UNII: 4NM5039Y5X)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59900-208-01	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2008
2	NDC: 59900-208-02	208175 mL in 1 DRUM; Type 0: Not a Combination Product	02/01/2008
3	NDC: 59900-208-03	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2008
4	NDC: 59900-208-04	1000 mL in 1 BAG; Type 0: Not a Combination Product	02/01/2008
5	NDC: 59900-208-05	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2008
6	NDC: 59900-208-06	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2008
7	NDC: 59900-208-07	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2008
8	NDC: 59900-208-08	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/01/2008
9	NDC: 59900-208-09	946250 mL in 1 DRUM; Type 0: Not a Combination Product	02/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/01/2008

Labeler - Best Sanitizer, Inc. (957473614)

Establishment
Name	Address	ID/FEI	Business Operations
Best Sanitizer, Inc.		627278224	manufacture(59900-208)