NDC 49035-552 - Ear Wax Removal System
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 49035-552
- Package NDCs from labels
- 49035-552-01
- Manufacturer
- Walmart | Product Quest Mfg
- Effective date
- 2018-01-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ear Wax Removal Drops Well at Walgreens - Walmart | Product Quest Mfg | Walmart | Product Quest Mfg | 2018-01-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49035-552-01 | Ear Wax Removal System | 15 mL in 1 BOTTLE | SOLUTION/ DROPS | 15 mL | 6.5 g in 100mL | 3 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Carbamide Peroxide | ACTIVE INGREDIENT | 31PZ2VAU81 | EAR WAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE - 6.50%) KIT [WALMART] | 1 | |
| HYDROGEN PEROXIDE | ACTIVE MOIETY | BBX060AN9V | EAR WAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE - 6.50%) KIT [WALMART] | 1 | |
| ALOE VERA LEAF | INACTIVE INGREDIENT | ZY81Z83H0X | EAR WAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE - 6.50%) KIT [WALMART] | 1 | |
| CHAMOMILE | INACTIVE INGREDIENT | FGL3685T2X | EAR WAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE - 6.50%) KIT [WALMART] | 1 | |
| Glycerin | INACTIVE INGREDIENT | PDC6A3C0OX | EAR WAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE - 6.50%) KIT [WALMART] | 1 | |
| Oxyquinoline Sulfate | INACTIVE INGREDIENT | 61VUG75Y3P | EAR WAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE - 6.50%) KIT [WALMART] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.