AURORA
- Product NDC
- 63148-104
- 11-digit product format
- 631480104
- Labeler code
- 63148
- Product ID
- 63148-104_cdf8f314-db1e-4273-87c7-f5030a01d734
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRICLOSAN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- APOLLO HEALTH AND BEAUTY CARE
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-01-13
- Marketing end
- 0000-00-00
- Substance
- TRICLOSAN
- Active strength
- 5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63148-104-08 | AURORAANTIBACTERIAL COCONUT TROPICAL ISLAND | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63148-104 | AURORA ANTIBACTERIAL COCONUT TROPICAL ISLAND (TRICLOSAN) LIQUID [APOLLO HEALTH AND BEAUTY CARE] | 1 | Legacy NDC, 1 package rows | 20150115_d4df6cf3-3afc-4a74-a2d3-4452557b3330.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63148-104-08 | 63148010408 | 237 mL in 1 BOTTLE, PLASTIC | 237 ml | Historical |