Antibacterial Liquid Hand
- Product NDC
- 51143-541
- 11-digit product format
- 511430541
- Labeler code
- 51143
- Product ID
- 51143-541_1412fee9-1ac0-472d-868c-542a1db339b8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRICLOSAN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- OnPoint, Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2009-07-30
- Marketing end
- 0000-00-00
- Substance
- TRICLOSAN
- Active strength
- 0 kg/100L
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| TRICLOSAN | ACTIVE INGREDIENT | 4NM5039Y5X | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| TRICLOSAN | ACTIVE MOIETY | 4NM5039Y5X | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| COCAMIDOPROPYL BETAINE | INACTIVE INGREDIENT | 5OCF3O11KX | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| DMDM HYDANTOIN | INACTIVE INGREDIENT | BYR0546TOW | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| PEG-120 METHYL GLUCOSE DIOLEATE | INACTIVE INGREDIENT | YM0K64F20V | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| SODIUM LAURETH SULFATE | INACTIVE INGREDIENT | BPV390UAP0 | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | ANTIBACTERIAL LIQUID HAND (TRICLOSAN) LIQUID [ONPOINT, INC] | 1 | |