FDA.reportPublic FDA data

NDC 0316-0201 - Dermasorb HC Complete Kit

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
0316-0201
Package NDCs from labels
0316-0201-01
Manufacturer
Crown Laboratories
Effective date
2019-09-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hydrocortisone Lotion with Shampoo and Body Wash - Crown LaboratoriesCrown Laboratories2019-09-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HYDROCORTISONE ACETATEACTIVE INGREDIENT3X7931PO74DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]1
HYDROCORTISONEACTIVE MOIETYWI4X0X7BPJDERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]1
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W7DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]1
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]1
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YHDERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3DERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]1
WATERINACTIVE INGREDIENT059QF0KO0RDERMASORB HC COMPLETE KIT (HYDROCORTISONE LOTION WITH SHAMPOO AND BODY WASH) KIT [CROWN LABORATORIES]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.

Matched openFDA labels page 129 of 229 · 4,568 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MGC Health Cough Drops Original HerbMENTHOLMedical Group Care LLC3d70ba70-eb11-f148-e063-6294a90a4c7c2025-08-28WarningsExact identifier
unii: L7T10EIP3A
Mountain Ice Pain ReliefMENTHOLMountainside Medical Equipment, Inc.c79fdd91-16f4-4ae0-bee4-d37c05ed20742025-08-28WarningsExact identifier
unii: L7T10EIP3A
Exchange Select Cough Drops Original HerbMENTHOLArmy & Air Force Exchange Service3d7109a5-4fe1-039b-e063-6394a90a13922025-08-28WarningsExact identifier
unii: L7T10EIP3A
MGC Health Drops Sugar Free Lemon MintMENTHOLMedical Group Care LLC3d70bca7-e830-e693-e063-6294a90a73f92025-08-28WarningsExact identifier
unii: L7T10EIP3A
Exchange Select Drops Sugar Free Lemon MintMENTHOLArmy & Air Force Exchange Service3d70450f-04ea-1885-e063-6294a90a05bd2025-08-28WarningsExact identifier
unii: L7T10EIP3A
MGC Health Cough Drops Honey HerbMENTHOLMedical Group Care LLC3d710deb-e42d-13eb-e063-6394a90a56e12025-08-28WarningsExact identifier
unii: L7T10EIP3A
HealthWise Overnight Menthol PatchMENTHOLVeridian Healthcare6379f50d-2878-46ca-8acb-71c4554585e92025-08-28WarningsExact identifier
unii: L7T10EIP3A
Sterile WaterWATER INJECTIONHenry Schein, Inc.3501952b-b556-4d5e-b81b-5c35ff87b4752025-08-28Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Anti Itch Maximum ReliefPRAMOXINE HYDROCHLORIDE AND MENTHOLNatureplex LLC75de3d5e-ecbe-4d04-a39d-792200e6ee322025-08-28WarningsExact identifier
unii: L7T10EIP3A
ARCTIC HEATMENTHOL, METHYL SALICYLATERenu Laboratories, LLC402df5c1-b8cb-17a2-e054-00144ff8d46c2025-08-27WarningsExact identifier
unii: L7T10EIP3A
wet wipes 01BENZALKONIUM CHLORIDECosmuses Cosmetics (Ningbo) Co., Ltd.3d3d7e8b-1ec1-9f9f-e063-6294a90ade0e2025-08-25WarningsExact identifier
unii: F5UM2KM3W7
Foaming Facial CleanserGLYCERIN, NIACINAMIDEGuangzhou Danting Bath&Body Care Industry Co. Ltd396c1db9-a5d3-cc82-e063-6294a90a90bb2025-08-23WarningsExact identifier
unii: PDC6A3C0OX
Burn CreamBENZALKONIUM CHLORIDE, LIDOCAINE HCITrifecta Pharmaceuticals USA LLCfe439c60-5a02-648f-e053-6294a90a14032025-08-23WarningsExact identifier
unii: F5UM2KM3W7
OP-First Aid Series ALCOHOL PREP PADS STERILEISOPROPYL ALCOHOL CLOTHYiwu Ori-Power Medtech Co.,Ltd.351f4b1e-75c9-abec-e063-6294a90a28752025-08-22WarningsExact identifier
unii: ND2M416302
YehealCAMPHOR, MENTHOL, ISOPROPYL ALCOHOLShenzhen Yeheal Biotechnology Co., Ltd3cf1bc74-3060-6d63-e063-6294a90a9f5c2025-08-22WarningsExact identifier
unii: L7T10EIP3A
unii: ND2M416302
70% ISOPROPYL RUBBING ALCOHOL WITH WINTERGREENISOPROPYL ALCOHOLJell Pharmaceuticals Pvt. Ltd.3cf2ff12-0220-3307-e063-6394a90abf082025-08-22WarningsExact identifier
unii: ND2M416302
Chain Drug Marketing Association, Inc.ISOPROPYL ALCOHOLChain Drug Marketing Association Inc.18fe4787-8986-4d64-e063-6394a90a35132025-08-22WarningsExact identifier
unii: ND2M416302
Refresh RELIEVA PFCARBOXYMETHYLCELLULOSE SODIUM AND GLYCERINAllergan, Inc.d5d3df4a-a311-4f2d-9a24-edfec1a6c9f92025-08-22WarningsExact identifier
unii: PDC6A3C0OX
Refresh OptiveCARBOXYMETHYLCELLULOSE SODIUM, GLYCERINAllergan, Inc.37e99aa8-02d6-4efb-a862-90bc7fcd5ca52025-08-22WarningsExact identifier
unii: PDC6A3C0OX
AMERICAN REDCROSS 70% ISOPROPYL RUBBING ALCOHOLISOPROPYL ALCOHOLMY IMPORTS USA LLCd4d7d0e8-12b4-e410-e053-2a95a90a7f302025-08-21WarningsExact identifier
unii: ND2M416302

Reported adverse events (FAERS/openFDA)#

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