Label: DIAL ANTIBACTERIAL BAR- dial mountain fresh antibacterial bar soap soap
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NDC Code(s):
54340-274-01,
54340-274-02,
54340-274-03,
54340-274-04, view more54340-274-05, 54340-274-06, 54340-274-07, 54340-274-08, 54340-274-09, 54340-274-10
- Packager: Henkel Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 14, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warning
- Keep out of reach of children
- Directions
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Inactive Ingredient
Soap [Sodium Tallowate*, Sodium Palmate*, Sodium Cocoate*, Sodium Palm Kernelate*], Aqua (Water, Eau), Talc, 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), CI 19140 (Yellow 6), CI 42053 (Green 3), *Contains one or more of these ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIAL ANTIBACTERIAL BAR
dial mountain fresh antibacterial bar soap soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-274 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) 8.01 g in 100 g WATER (UNII: 059QF0KO0R) 13.88 g in 100 g ALCOHOL (UNII: 3K9958V90M) 0.01 g in 100 g SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.388 g in 100 g SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) 10.93 g in 100 g TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.058 g in 100 g FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) 0.0016 g in 100 g BASIC YELLOW 57 (UNII: 4N63359G0X) 0.009 g in 100 g STEARIC ACID (UNII: 4ELV7Z65AP) 2.42 g in 100 g SODIUM PALMATE (UNII: S0A6004K3Z) 61.47 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.8 g in 100 g SORBITOL (UNII: 506T60A25R) 0.55 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-274-01 180 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 2 NDC:54340-274-02 339 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 3 NDC:54340-274-03 452 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 4 NDC:54340-274-04 678 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 5 NDC:54340-274-05 540 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 6 NDC:54340-274-06 940 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 7 NDC:54340-274-07 1130 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 8 NDC:54340-274-08 1356 g in 1 CELLO PACK; Type 0: Not a Combination Product 07/01/2017 9 NDC:54340-274-09 339 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 10 NDC:54340-274-10 904 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 07/01/2017 Labeler - Henkel Corporation (080887708)