DIAL ANTIBACTERIAL BAR- dial white antibacterial bar soap soap 
Henkel Corporation

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Dial Antibacterial Deodarant Bar Soap - White

Active Ingredient

Benzalkonium Chloride 0.10%

Purpose

Antibacterial

Uses

Warnings

For external use only

When using this product

  • avoid contact with eyes. In case of eye contact, flush with water.

Stop using and ask doctor if

  • irritation or redness develops

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Center right away.

Directions

Inactive ingredients

Soap [Sodium Tallowate* • Sodium Palmate* • Sodium Cocoate* • Sodium Palm Kernelate*] • Aqua (Water, Eau) • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Tallow Acid* • Glycerin • PEG-6 Methyl Ether • Parfum (Fragrance) • Sodium Chloride • Pentasodium Pentetate • Tetrasodium Etidronate • CI 77891 (Titanium Dioxide)

*Contains one or more of these ingredients

Questions?

1-800-258-DIAL (3425)

54340-278-07 (12B 4oz - 2398448)

54340-278-06 (10B 4oz - 2343044)

54340-278-05 (8B 4oz - 2343032)

54340-278-02 (3B 4oz - 2342060)

54340-278-01 (2B 3.2oz - 2342054)

DIAL ANTIBACTERIAL BAR 
dial white antibacterial bar soap soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-278
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.8 g  in 100 g
SORBITOL (UNII: 506T60A25R) 0.5525 g  in 100 g
SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.3898 g  in 100 g
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) 11.01 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX) 8.1 g  in 100 g
ALCOHOL (UNII: 3K9958V90M) 0.01 g  in 100 g
SODIUM PALMATE (UNII: S0A6004K3Z) 61.87 g  in 100 g
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.058 g  in 100 g
STEARIC ACID (UNII: 4ELV7Z65AP) 2.4365 g  in 100 g
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54340-278-10113 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
2NDC:54340-278-11339 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
3NDC:54340-278-09904 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
4NDC:54340-278-061130 g in 1 CELLO PACK; Type 0: Not a Combination Product07/01/201702/07/2023
5NDC:54340-278-081356 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
6NDC:54340-278-04678 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2023
7NDC:54340-278-19181 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2020
8NDC:54340-278-12452 g in 1 CELLO PACK; Type 0: Not a Combination Product01/31/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)07/01/2017
Labeler - Henkel Corporation (080887708)

Revised: 11/2023
Document Id: 09d2bc09-6d92-bcf9-e063-6294a90af0a2
Set id: 5691b718-bb66-1529-e054-00144ff88e88
Version: 8
Effective Time: 20231110
 
Henkel Corporation