DAWNMIST DEODORANT- triclosan soap 
Dukal Corporation

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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DawnMist Deodorant Soap

Active Ingredient

Triclosan 0.20%

Purpose

Antibacterial

Use

For handwashing to decrease bacteria on skin.

Warning

For external use only

  • Do not use in eyes
  • Discontinue use if redness or irritation develops
  • Use only as directed

Keep out of reach of children


Directions

Wet bar with water

Lather vigorously and wash skin

Rinse and dry thoroughly

Other Ingredients

Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Sodium Chloride, Fragrance,
Tetrasodium EDTA

Package Label

DawnMist

Gentle Formula French Milled

Contains Antibacterial Agent Triclosan

Lightly Scented

Deodorant Soap

Vegetable based product

Manufactured for: DUKAL CORPORATION, Ronkonkoma, NY 11779
(631)656-3800 www.dukal.com

Reorder No. ASP4128

Made in USA


label


DAWNMIST DEODORANT 
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-1013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SODIUM PALMATE (UNII: S0A6004K3Z)  
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
EDETATE SODIUM (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65517-1013-111 g in 1 PACKAGE; Type 0: Not a Combination Product01/08/201301/08/2013
2NDC:65517-1013-218 g in 1 PACKAGE; Type 0: Not a Combination Product01/08/201301/08/2013
3NDC:65517-1013-325 g in 1 PACKAGE; Type 0: Not a Combination Product01/08/201301/08/2013
4NDC:65517-1013-435 g in 1 PACKAGE; Type 0: Not a Combination Product01/08/201301/08/2013
5NDC:65517-1013-576 g in 1 PACKAGE; Type 0: Not a Combination Product01/08/201301/08/2013
6NDC:65517-1013-6127 g in 1 PACKAGE; Type 0: Not a Combination Product01/08/201301/08/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/08/201301/08/2013
Labeler - Dukal Corporation (791014871)

Revised: 9/2018
 
Dukal Corporation