OTC - ACTIVE INGREDIENT SECTION
Active Ingredient - Triclosan 0.115%
Antibacterial
- Manufacturer
- Brands International Corp
- Effective date
- 2016-05-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:47:43
Label at a glance#
ProductAntibacterial
Active ingredientTRICLOSAN
Label structure10 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Purpose - Antibacterial
INDICATIONS & USAGE SECTION
Use for handwashing to decrease bacteria on the skin
WARNINGS SECTION
Warnings
For external use only - hands only
OTC - WHEN USING SECTION
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or redness develops n condition persists for more than 72 hours
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 hands
- apply palmful to hands
- scrub thoroughly
- rinse thoroughly
INACTIVE INGREDIENT SECTION
Inactive Ingredients - Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Fragrance (Parfum), Sodium Lauroamphoacetate, Polyquaternium 7, Glycerin, Citric Acid, Aloe Barbadensis Leaf Extract, Tocopheryl (Vitamin E) Acetate, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5 (Cl 19140), Red 4 (Cl 14700)
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50157-201-24 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-2c2e-a910-e053-dadaa90a0b85 | 3f8e32da-7ccc-605a-e054-00144ff88e88 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50157-201-24 | Antibacterial | 709 mL in 1 BOTTLE | LIQUID | 709 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Antibacterial
- Triclosan
- METHYLISOTHIAZOLINONE
- FD&C YELLOW NO. 5
- FD&C RED NO. 4
- METHYLCHLOROISOTHIAZOLINONE
- WATER
- SODIUM LAURETH SULFATE
- SODIUM CHLORIDE
- COCAMIDOPROPYL BETAINE
- SODIUM LAUROAMPHOACETATE
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)
- GLYCERIN
- ANHYDROUS CITRIC ACID
- ALOE VERA LEAF
- .ALPHA.-TOCOPHEROL ACETATE, DL-
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50157-201 | 50157-201-24 |
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 |
|---|---|---|---|---|---|---|
| 3f8e32da-7ccd-605a-e054-00144ff88e88 | 3f8e32da-7ccc-605a-e054-00144ff88e88 | 2016-05-06 | Warnings | 3f8e32da-7ccd-605a-e054-00144ff88e88 3f8e32da-7ccc-605a-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.