Earwax Removal
- Product NDC
- 49762-450
- 11-digit product format
- 497620450
- Labeler code
- 49762
- Product ID
- 49762-450_41cd1174-13f5-4a50-8955-9f1cf9fc398e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Earwax Removal
- Dosage form
- LIQUID
- Route
- AURICULAR (OTIC)
- Labeler
- Apothecary Products, LLC
- Application
- part344
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2008-08-31
- Marketing end
- 0000-00-00
- Substance
- CARBAMIDE PEROXIDE
- Active strength
- 7 mg/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49762-450-15 | Earwax Removal | 15 mL in 1 BOTTLE | LIQUID | 15 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49762-450 | EARWAX REMOVAL LIQUID [APOTHECARY PRODUCTS, LLC] | 2 | Legacy NDC, 1 package rows | 20140527_a07ccd1b-02e7-41f8-873d-7a7b7eddec16.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49762-450-15 | 49762045015 | 15 mL in 1 BOTTLE | 15 ml | Historical |