Label: DIAL COMPLETE ANTIBACTERIAL BAR SPRING WATER- benzalkonium chloride soap
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NDC Code(s):
54340-270-08,
54340-270-12,
54340-270-13,
54340-270-14, view more54340-270-15, 54340-270-16, 54340-270-17, 54340-270-18, 54340-270-19
- Packager: Henkel Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients Soap (Sodium Tallowate* • Sodium Palmate* • Sodium Cocoate* • Sodium Palm Kernelate*) • Aqua (Water, Eau) • Glycerin • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Stearic Acid* • Tallow Acid* • Parfum (Fragrance) • Sorbitol • CI77891 (Titanium Dioxide) • Sodium Chloride • Tetrasodium Glutamate Diacetate • Alcohol
*Contains one or more of these ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DIAL COMPLETE ANTIBACTERIAL BAR SPRING WATER
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54340-270 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 WATER (UNII: 059QF0KO0R) 13.95 g in 100 g SODIUM CHLORIDE (UNII: 451W47IQ8X) 0.39 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) 8.05 g in 100 g SODIUM PALMATE (UNII: S0A6004K3Z) 61.81 g in 100 g STEARIC ACID (UNII: 4ELV7Z65AP) 2.434 g in 100 g ALCOHOL (UNII: 3K9958V90M) 0.01 g in 100 g SODIUM PALM KERNELATE (UNII: 6H91L1NXTW) 11 g in 100 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.8 g in 100 g SORBITOL (UNII: 506T60A25R) 0.5525 g in 100 g TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 0.058 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54340-270-08 8 in 1 PACKAGE 03/08/2021 1 113 g in 1 PACKET; Type 0: Not a Combination Product 2 NDC:54340-270-12 12 in 1 PACKAGE 03/08/2021 2 113 g in 1 PACKET; Type 0: Not a Combination Product 3 NDC:54340-270-13 113 g in 1 PACKET; Type 0: Not a Combination Product 01/31/2023 4 NDC:54340-270-14 1356 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 5 NDC:54340-270-15 904 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 6 NDC:54340-270-16 339 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 7 NDC:54340-270-17 181 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 8 NDC:54340-270-18 678 g in 1 CELLO PACK; Type 0: Not a Combination Product 01/31/2023 9 NDC:54340-270-19 452 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) 03/08/2021 Labeler - Henkel Corporation (080887708)