Auro Ear Wax Remover
- Product NDC
- 63736-232
- 11-digit product format
- 637360232
- Labeler code
- 63736
- Product ID
- 63736-232_017403c5-1be2-46a2-a6eb-63d15265d4ca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carbamide peroxide
- Dosage form
- LIQUID
- Route
- AURICULAR (OTIC)
- Labeler
- Insight Pharmaceuticals LLC
- Application
- part344
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-07-01
- Marketing end
- 0000-00-00
- Substance
- CARBAMIDE PEROXIDE
- Active strength
- 1 mL/22mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 63736-232-24 | Auro Ear Wax Remover | 22 mL in 1 TUBE | LIQUID | 22 | | 2 |
| 63736-232-24 | Auro Ear Wax Remover | 1 in 1 BOX | LIQUID | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63736-232 | AURO EAR WAX REMOVER (CARBAMIDE PEROXIDE) LIQUID [INSIGHT PHARMACEUTICALS LLC] | 2 | Legacy NDC, 2 package rows | 20110303_924e613b-4952-4861-aac7-b8534ea0f305.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63736-232-24 | 63736023224 | 22 mL in 1 TUBE | 22 ml | Historical |