DIAL PROFESSIONAL FOAMING HAND SANITIZER- dial professional foaming hand sanitizer liquid
Zotos International Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dial Professional Foaming Hand Sanitizer

DRUG FACTS

Active Ingredient(s)

Ethyl Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from fire or flame

When using this product avoid contact with face, eyes, and broken skin. if eye contact occurs, flush thoroughly with water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Put foam into DRY hands, wet hands thoroughly and rub into skin until dry.
Children under 6 years of age should be supervised by an adult when using this product.

Inactive ingredients

Aqua (Water, Eau)· PEG-10 Dimethicone · Glycerin · Cocamidopropyl PG-Dimonium Chloride· lsopropyl Myristate ·
PEG-12 Allyl Ether· T-Butyl Alcohol · Diazolidinyl Urea · Methylparaben

Questions

1-877-777-3277

Legal Entity

Package Label - Principal Display Panel

Front back 450 mL NDC: 50663-004-01

DIAL PROFESSIONAL FOAMING HAND SANITIZER
dial professional foaming hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50663-004
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62.75 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
METHYLPARABEN (UNII: A2I8C7HI9T)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE (UNII: 205Z54J075)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
GLYCERIN (UNII: PDC6A3C0OX)	0.857 mL in 100 mL
WATER (UNII: 059QF0KO0R)	33.97 mL in 100 mL

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50663-004-01	450 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/01/2020

Labeler - Zotos International Inc (966706145)