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 |
|---|---|---|---|---|---|---|
| Triple Antibiotic Plus Pain Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | FRED'S, INC. | a44db5d1-7a74-44aa-9aa7-6247e771aaf2 | 2025-07-15 | Warnings | 88AYB867L5 |
| Shopko Triple Antibiotic plus Pain Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Shopko Stores Operating Co., LLC | 5a9b2ea4-9b9d-4147-8aa0-7313d6be2cfa | 2025-07-15 | Warnings | 88AYB867L5 |
| sunmark triple antibiotic plus pain relief | POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE | Strategic Sourcing Services LLC | 941a6a71-e898-4af3-989a-6d3aa3224338 | 2025-07-15 | Warnings | 88AYB867L5 |
| TopCare Triple Antibiotic Plus Pain Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Topco Associates LLC | 0fc0dbc6-ca1d-42be-8016-68e64f119706 | 2025-07-15 | Warnings | 88AYB867L5 |
| Triple Antibiotic Plus Pain Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Walgreen Company | e2b7fc5b-c796-4ed1-aea7-4c810df250d5 | 2025-07-15 | Warnings | 88AYB867L5 |
| Publix antibiotic plus Pain Relief | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Publix Super Markets Inc | d0193bf1-a257-490e-a058-5e6a514981da | 2025-07-15 | Warnings | 88AYB867L5 |
| Gas-X Total Relief Maximum Strength | CALCIUM CARBONATE, SIMETHICONE | Haleon US Holdings LLC | edb0f11a-bdb7-484d-9257-09ff47b0fca4 | 2025-07-15 | Warnings | 92RU3N3Y1O |
| ProCure Moisture Barrier | 1% DIMETHICONE, 12% ZINC OXIDE | Twin Med LLC | 3988c83b-d4eb-1f09-e063-6394a90a45ad | 2025-07-14 | Warnings | 92RU3N3Y1O |
| Nikzon Hemorrhoidal | GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, AND PRAMOXINE HYDROCHLORIDE | Genomma Lab USA | 8f9a9939-2c99-489f-b597-9a51ec2684f9 | 2025-07-14 | Warnings | 88AYB867L5 |
| Antibiotic Plus Pain Relief | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | TARGET Corporation | 6fba5890-f48f-4302-a8ac-5087a6e03bd5 | 2025-07-11 | Warnings | 88AYB867L5 |
| TopCare Antibiotic Plus Pain Relief | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Topco Associates LLC | 55dc4025-f07f-41b2-8b18-6a11ee04b5cc | 2025-07-11 | Warnings | 88AYB867L5 |
| Sterile Water | STERILE WATER | Nephron Pharmaceuticals Corporation | bc04a883-babc-87a6-e053-2995a90a3dfd | 2025-07-11 | Warnings, Adverse reactions | 059QF0KO0R |
| REGULAR STRENGTH ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | WALGREEN COMPANY | 7cd9234e-d1cc-4cce-e053-2991aa0a457e | 2025-07-09 | Warnings | 92RU3N3Y1O |
| Maximum Strength Hemorrhoidal Cream with Aloe | GLYCERIN, PHENYLEPHINE HCI, PRAMOXINE HCI, PETROLATUM | Chain Drug Marketing Association | 396ea654-8be1-591a-e063-6294a90a11e2 | 2025-07-08 | Warnings | 88AYB867L5 |
| Aluminum Hydroxide, Magnesium Hydroxide, and Simethicone | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | Major Pharmaceuticals | 1bc90fa7-fcce-4a9b-862f-f30ab602ecab | 2025-07-07 | Warnings | 92RU3N3Y1O |
| Curist Gas Relief | SIMETHICONE | Little Pharma. Inc. | 3948c0e5-4ee7-5443-e063-6294a90ad6ae | 2025-07-06 | Warnings | 92RU3N3Y1O |
| Hemorrhoidal Cream | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Trifecta Pharmaceuticals Usa Llc | 38cf4e43-280b-eb96-e063-6294a90a5949 | 2025-07-02 | Warnings | 88AYB867L5 |
| TRIPLE ANTIBIOTIC PLUS PAIN RELIEF | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | GENOMMA LAB USA, INC. | 506fcda5-df44-49c8-8dbd-cab7434b06b2 | 2025-07-02 | Warnings | 88AYB867L5 |
| Curad Maximum Strength Triple Antibiotic | BACITRACIN, NEOMYCIN, POLYMYXIN B, PRAMOXINE HYDROCHLORIDE | Medline Industries, LP | 99e9c394-ebf1-7a27-e053-2a95a90ab157 | 2025-07-01 | Warnings | 88AYB867L5 |
| Exemax Cream | DIMETHICONE, ALLANTOIN | PureTek Corporation | 38e79055-df84-d314-e063-6394a90ac95f | 2025-07-01 | Warnings | 92RU3N3Y1O |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.