Earwax Removal Kit
- Product NDC
- 62011-0169
- 11-digit product format
- 620110169
- Labeler code
- 62011
- Product ID
- 62011-0169_9144cd5d-32fc-46c9-ab5d-ad364894d321
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Earwax Removal Kit
- Dosage form
- LIQUID
- Route
- AURICULAR (OTIC)
- Labeler
- McKesson
- Application
- part344
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-02-06
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62011-0169-1 | Earwax Removal Kit | 15 mL in 1 BOTTLE | LIQUID | 15 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62011-0169 | EARWAX REMOVAL KIT LIQUID [MCKESSON] | 4 | Legacy NDC, 1 package rows | 20120525_5c7b9c96-4429-4903-8f69-1bc26392a605.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62011-0169-1 | 62011016901 | 15 mL in 1 BOTTLE | 15 ml | Historical |