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 |
|---|---|---|---|---|---|---|
| Anti-Gas Ultra Strength | SIMETHICONE | Best Choice (Valu Merchandisers Company) | f74d9882-cc99-41b6-b851-ce89d28f33df | 2024-02-15 | Warnings | 92RU3N3Y1O |
| EPIFOAM | PRAMOXINE HYDROCHLORIDE AND HYDROCORTISONE ACETATE | Viatris Specialty LLC | b22b8b41-2f1e-11e4-8c21-0800200c9a66 | 2024-02-15 | Warnings, Adverse reactions | 88AYB867L5 |
| Blistex Medicated Mint Balm | DIMETHICONE, OCTINOXATE, AND OCTISALATE | Blistex Inc | 86fc9f3c-e35f-4988-bf19-64d9c6c85ee9 | 2024-02-09 | Warnings | 92RU3N3Y1O |
| Blistex Medicated Berry Balm | DIMETHICONE, OCTINOXATE, AND OCTISALATE | Blistex Inc | 827365b3-b3a5-4472-9add-f822362c4731 | 2024-02-09 | Warnings | 92RU3N3Y1O |
| Blistex Medicated Lip Balm | DIMETHICONE, OCTINOXATE, AND OCTISALATE | Blistex Inc | 8b4160ed-8889-4e3a-947f-a56c3324dbbe | 2024-02-09 | Warnings | 92RU3N3Y1O |
| REGULAR STRENGTH ANTACID AND ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | STRATEGIC SOURCING SERVICES LLC | fe04c244-d9b8-2800-e053-6294a90aeedc | 2024-02-06 | Warnings | 92RU3N3Y1O |
| Mylanta Classic | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE | Infirst Healthcare Inc. | 10a4cf29-39ed-87c3-e063-6394a90a4973 | 2024-02-05 | Warnings | 92RU3N3Y1O |
| Mylanta Vanilla Caramel | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE | Infirst Healthcare Inc. | 10a66d74-74b4-3f8d-e063-6394a90a7f00 | 2024-02-05 | Warnings | 92RU3N3Y1O |
| Right Remedies Maximum Strength Gas Relief Softgel | SIMETHICONE | Strive Pharmaceuticals Inc. | 032b3a89-1bc4-4f38-ba9e-0a4840215330 | 2024-02-05 | Warnings | 92RU3N3Y1O |
| Sterile Water | STERILE WATER | Chartwell RX, LLC | 3681eeaa-807a-47ca-9fbc-61c2b682800a | 2024-02-01 | 059QF0KO0R | |
| Sterile Water | WATER | A-S Medication Solutions | dba87371-31d2-47c2-ab83-89aabce4b184 | 2024-01-31 | Warnings, Adverse reactions | 059QF0KO0R |
| XtraCare Skin Relief Oatmeal Daily Moisturizing | DIMETHICONE | Rejoice International | 8d9e0893-c9be-4f5a-afc2-b5b997c8d1cc | 2024-01-29 | Warnings | 92RU3N3Y1O |
| Antibiotic and Pain Relief | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Target Corporation | 050be94c-1fbb-4d84-82c6-841aac8f318e | 2024-01-18 | Warnings | 88AYB867L5 |
| Multi-Action Antibiotic and Pain Relief | BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE OINTMENT | Target Corporation | 8fecff32-bd67-4351-90f7-0c28cb335ea3 | 2024-01-18 | Warnings | 88AYB867L5 |
| Triple Antibiotic and Pain Relief | TRIPLE ANTIBIOTIC | Target Corporation | 8fda7b8a-72f3-4b92-a229-ac5be0e3b3eb | 2024-01-17 | Warnings | 88AYB867L5 |
| Sunmark Caldiphen | CALAMINE AND PRAMOXINE HYDROCHLORIDE | Strategic Sourcing Services | 4f4d4c54-64b5-4e20-bed0-c7fb470b8434 | 2024-01-12 | Warnings | 88AYB867L5 |
| EIGHT HOUR NIGHT | DIMETHICONE | REVLON | b3b277f9-565a-636c-e053-2995a90a94d2 | 2024-01-12 | Warnings | 92RU3N3Y1O |
| Maximum Strength Gas Relief Softgel | SIMETHICONE | Cardinal Health 110, LLC. DBA Leader | 57043cae-a8db-4eff-835c-5995e8aea924 | 2024-01-11 | Warnings | 92RU3N3Y1O |
| Prosoria Anti-Itch Moisturizer | PRAMOXINE HYDROCHLORIDE | Nuvothera, Inc. | 3c4b9515-f435-4227-a347-d6508778426d | 2024-01-10 | Warnings | 88AYB867L5 |
| F02 ANGR-FLX | ADELHEID AQUA, ARSENICUM ALBUM, BIG SAGEBRUSH, BOS TAURUS LIVER, GALLBLADDER, BRIZA MAXIMA, CALENDULA OFFICINALIS, CAYENNE, CHAMOMILE , CHICORY , GARLIC, ENGLISH HOLLY , EUROPEAN BEECH , FORKING LARKSPUR , GERMAN CHAMOMILE , IMPATIENS GLANDULIFERA , JUGLANS REGIA , LILIUM TIGRINUM, MORNING GLORY, MOUNTAIN DOGWOOD, NATRUM MURIATICUM, NUX VOMICA, PINUS SYLVESTRIS , REDWOOD, RUBBER RABBITBRUSH, SEPIA, TOLMIE STAR TULIP, VERBENA OFFICINALIS , VITIS VINIFERA , WATERMELON, WHITE WILLOW , YELLOW STAR THISTLE | Apex Energetics Inc. | bc7c2bf3-8b0d-766f-e053-2a95a90ad34c | 2024-01-08 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.