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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Walgreens Multi-Antibiotic with Pain Relief Cream | POLYMYXIN B SULFATE, NEOMYCIN SULFATE, PRAMOXINE HYDROCHLORIDE | Walgreens Company | f4feccc3-ac25-4d8a-9b68-9a24f755524a | 2024-11-20 | Warnings | 88AYB867L5 |
| Walgreens Kids Multi-Antibiotic with Pain Relief Cream | POLYMYXIN B SULFATE, NEOMYCIN SULFATE, PRAMOXINE HYDROCHLORIDE | Walgreens Company | fbc364d7-d8b8-43f5-99cc-290438f3982b | 2024-11-20 | Warnings | 88AYB867L5 |
| Gas-Aid | SIMETHICONE | Leosons Overseas Corp | d271bfcb-bf13-4a97-bc03-f1824826f15a | 2024-11-19 | Warnings | 92RU3N3Y1O |
| Gas-Aid Drops for infants | SIMETHICONE | Leosons Overseas Corp | 06665701-5f1c-4f8f-8775-e0a4a9ef2029 | 2024-11-19 | Warnings | 92RU3N3Y1O |
| Potassium Citrate and Citric Acid | POTASSIUM CITRATE AND CITRIC ACID MONOHYDRATE | PAI Holdings, LLC dba PAI Pharma | ce42122f-8087-471f-b0a3-5524bdbd4526 | 2024-11-19 | Warnings, Adverse reactions | 2968PHW8QP |
| TRICITRATES | POTASSIUM CITRATE, SODIUM CITRATE, AND CITRIC ACID MONOHYDRATE | PAI Holdings, LLC dba PAI Pharma | 2ecb42a2-82f1-456b-8f1e-02c2d0a7b5ad | 2024-11-15 | Warnings, Adverse reactions | 2968PHW8QP |
| Sal de Uvas Picot | CITRIC ACID MONOHYDRATE AND SODIUM BICARBONATE | RB Health Mexico, S.A. de C.V. | 151b9bc9-1a6e-4401-ae58-4b4210ab4505 | 2024-11-15 | Warnings | 2968PHW8QP |
| TiZO Photoceutical Environmental Skin Protectant | DIMETHICONE | Fallien Cosmeceuticals, LTD | 84a3299d-9b98-492e-a83f-ebd72ec58f8d | 2024-11-14 | Warnings | 92RU3N3Y1O |
| Neosporin Pain Itch Scar | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 55392c48-b5d8-44cd-8c10-6d8668349848 | 2024-11-13 | Warnings | 88AYB867L5 |
| Neosporin Kids Plus Pain Relief | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 6752f0a0-2432-4d8b-8198-74ae96a68963 | 2024-11-13 | Warnings | 88AYB867L5 |
| Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 23222e54-d793-4d79-980e-550e32a95742 | 2024-11-13 | Warnings | 88AYB867L5 |
| Neosporin Plus Pain Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 32302dcd-f3f1-408b-ae5f-e7d8b666f68f | 2024-11-13 | Warnings | 88AYB867L5 |
| NEOSPORIN Plus BURN RELIEF | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 3caa7fd1-bd66-427e-a6c0-1b137b205089 | 2024-11-13 | Warnings | 88AYB867L5 |
| Triple Antibiotic and Burn Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE | CVS Pharmacy | fdc510b8-f3ad-4bd6-a8d0-1b81e9f30e13 | 2024-11-13 | Warnings | 88AYB867L5 |
| Mag-AL Plus XS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND DIMETHICONE | PAI Holdings, LLC dba PAI Pharma | db0c47ab-5296-4195-9fa6-2e338b665094 | 2024-11-12 | Warnings | 92RU3N3Y1O |
| basic care first aid antibiotic and burn relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE | Amazon.com Services LLC | 0df4c44d-6912-4db9-a703-a82da4c8ae76 | 2024-11-11 | Warnings | 88AYB867L5 |
| Crane Safety Eye Wash | WATER SOLUTION | Crane Safety LLC | 96d8dda9-6cd6-3f68-e053-2995a90a0da2 | 2024-11-08 | Warnings | 059QF0KO0R |
| ABC Arbonne Baby Care Diaper Rash | DIMETHICONE AND ZINC OXIDE | Arbonne International, LLC | dd1d8198-bb9d-4508-a971-ae3bc624cdd1 | 2024-11-08 | Warnings | 92RU3N3Y1O |
| RUGBY EYE WASH | WATER, PURIFIED | A-S Medication Solutions | 0773e558-2f46-494c-888a-3bc517202b65 | 2024-11-08 | Warnings | 059QF0KO0R |
| Peviderm Pramoxine Hydrocholride 1% | PRAMOXINE HYDROCHLORIDE | Stratus Pharmaceuticals Inc | 680b40fa-1922-443a-a4b0-7c3f6a2b847d | 2024-11-07 | Warnings | 88AYB867L5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.