NDC 17030-040 - 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
17030-040
Package NDCs from labels
17030-040-16
Manufacturer
Vetoquinol USA, Inc. | Syn-Tech Chem. & Pharm. Co., Ltd. | Tropichem Research Labs, LLC dba Vetio
Effective date
2026-01-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dermal-Soothe™Vetoquinol USA, Inc. | Syn-Tech Chem. & Pharm. Co., Ltd. | Tropichem Research Labs, LLC dba Vetio2026-01-06OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17030-040-16Dermal-Soothe474 mL in 1 BOTTLE, PLASTICSHAMPOO4746

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17030-040DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]51 package rows20211214_b3fdf6a1-2ba2-45a4-b1f4-9241886ba025.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Pramoxine HydrochlorideACTIVE INGREDIENT88AYB867L5DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
PramoxineACTIVE MOIETY068X84E056DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Ammonium Laureth-2 SulfateINACTIVE INGREDIENT698O4Z48G6DERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Cetyl AlcoholINACTIVE INGREDIENT936JST6JCNDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Citric Acid MonohydrateINACTIVE INGREDIENT2968PHW8QPDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Cocamidopropyl HydroxysultaineINACTIVE INGREDIENT62V75NI93WDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Coco DiethanolamideINACTIVE INGREDIENT92005F972DDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Decyl GlucosideINACTIVE INGREDIENTZ17H97EA6YDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
Glycol StearateINACTIVE INGREDIENT0324G66D0EDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
OatmealINACTIVE INGREDIENT8PI54V663YDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
OcthilinoneINACTIVE INGREDIENT4LFS24GD0VDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
PEG-75 LanolinINACTIVE INGREDIENT09179OX7TBDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2
WaterINACTIVE INGREDIENT059QF0KO0RDERMAL-SOOTHE (PRAMOXINE HYDROCHLORIDE) SHAMPOO [VETOQUINOL USA, INC.]2

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.

Matched openFDA labels page 37 of 37 · 725 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MG217 Baby EczemaCOLLOIDAL OATMEALWisconsin Pharmacal Company5d65052d-2972-544d-e053-2a91aa0afa3e2017-11-28WarningsExact identifier
unii: 8PI54V663Y
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
First Degree Maximum Strength BurnPRAMOXINE HYDROCHLORIDEWelmedix LLC1afa337e-f411-42df-b2f5-5f72c9b52ffa2017-03-09WarningsExact identifier
unii: 88AYB867L5
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.