Dial Complete
- Manufacturer
- Henkel Corporation
- Effective date
- 2024-01-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:16:15
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active ingredient
Benzalkonium Chloride 0.1%
OTC - PURPOSE SECTION
Purpose
Antibacterial
INDICATIONS & USAGE SECTION
Use For washing to decrease bacteria on the skin.
WARNINGS SECTION
Warnings
For external use only
OTC - WHEN USING SECTION
When using this product avoid contact with the eyes. In case of eye contact, flush with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation and redness develops.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Directions
Wet bar with water. Lather vigorously and wash skin. Rinse and dry thoroughly.
INACTIVE INGREDIENT SECTION
Inactive ingredients Soap (Sodium Tallowate* • Sodium Palmate* • Sodium Cocoate* • Sodium Palm Kernelate*) • Water • Glycerin • Coconut Acid* • Palm Acid* • Palm Kernel Acid* • Stearic Acid* • Fragrance • Sorbitol • Sodium Chloride • Tetrasodium Glutamate Diacetate •Titanium Dioxide • Yellow 5 • Alcohol • Yellow 8 • Red 4
*Contains one or more of these ingredients
OTC - QUESTIONS SECTION
Questions? 1-800-258-DIAL (3425)
SPL UNCLASSIFIED SECTION
Visit our website at
www.dialsoap.com
Henkel®, TM, ©2021 Distributed by
Henkel Corporation, Rocky Hill, CT 06067
Made in Columbia
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Dial COMPLETE®
12 BARS
gold antibacterial
ELIMINATES 99% OF BACTERIA**
CLEAN RINSING, NON-DRYING
DEODORANT BAR SOAP
moisturizing conditioners
gentle cleansers
free from parabens, phthalates, silicones
12-4 OZ SOAP BARS (113 g) EACH, TOTAL NET WT 48 OZ (1.35 kg)
Products#
Every source-derived product name is available through these pages.
- Dial Complete Gold Antibacterial
- Benzalkonium Chloride
- FD&C RED NO. 4
- FD&C YELLOW NO. 5
- SODIUM PALMATE
- SODIUM COCOATE
- COCONUT ACID
- STEARIC ACID
- SORBITOL
- TETRASODIUM GLUTAMATE DIACETATE
- PALM ACID
- GLYCERIN
- WATER
- BENZALKONIUM
- PALM KERNEL ACID
- ALCOHOL
- TITANIUM DIOXIDE
- SODIUM CHLORIDE
- SODIUM PALM KERNELATE
- FLUORESCEIN SODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 54340-269 | 54340-269-12, 54340-269-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 0dfa4948-6ba4-bc88-e063-6294a90a87b6 | d9e2dfe9-2cf0-58b4-e053-2a95a90aa9a2 | 2024-01-01 | Warnings | 0dfa4948-6ba4-bc88-e063-6294a90a87b6 d9e2dfe9-2cf0-58b4-e053-2a95a90aa9a2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
