Label: DIAL PROFESSIONAL FOAMING HAND SANITIZER liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 50663-004-01 - Packager: Zotos International Inc
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated May 1, 2020
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- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredient(s)
- Purpose
- Use
- Warnings
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WHEN USING
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.
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive ingredients
- Questions
- Legal Entity
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
DIAL PROFESSIONAL FOAMING HAND SANITIZER
dial professional foaming hand sanitizer liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50663-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62.75 mL in 100 mL Inactive Ingredients Ingredient Name Strength 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 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50663-004-01 450 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/01/2020 Labeler - Zotos International Inc (966706145)