NDC 17030-041 - Dermal-Soothe
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
- 17030-041
- Package NDCs from labels
- 17030-041-12
- Manufacturer
- Vetoquinol USA, Inc. | Syn-Tech Chem. & Pharm. Co., Ltd. | Tropichem Research Labs, LLC dba Vetio
- Effective date
- 2024-12-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Micro Pearls ® Advantage Dermal-Soothe™ Spray | Vetoquinol USA, Inc. | Syn-Tech Chem. & Pharm. Co., Ltd. | Tropichem Research Labs, LLC dba Vetio | 2024-12-17 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17030-041-12 | Dermal-Soothe | 355 mL in 1 BOTTLE, PLASTIC | SPRAY | 355 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Pramoxine Hydrochloride | ACTIVE INGREDIENT | 88AYB867L5 | DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SPRAY [VETOQUINOL USA, INC.] | 1 | |
| Pramoxine | ACTIVE MOIETY | 068X84E056 | DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SPRAY [VETOQUINOL USA, INC.] | 1 | |
| Citric Acid Monohydrate | INACTIVE INGREDIENT | 2968PHW8QP | DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SPRAY [VETOQUINOL USA, INC.] | 1 | |
| N-Lactoyl Ethanolamine | INACTIVE INGREDIENT | 900T44YNC7 | DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SPRAY [VETOQUINOL USA, INC.] | 1 | |
| Quaternium-15 | INACTIVE INGREDIENT | E40U03LEM0 | DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SPRAY [VETOQUINOL USA, INC.] | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SPRAY [VETOQUINOL USA, INC.] | 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.