FDA.reportPublic FDA data

NDC 47682-397-99 - Hydrocortisone

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
47682-397
Requested NDC
47682-397-99
Package NDCs from labels
47682-397-71, 47682-397-12, 47682-397-99, 47682-397-73, 47682-397-35
Manufacturer
Unifirst First Aid Corporation
Effective date
2025-09-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hydrocortisone - Unifirst First Aid CorporationUnifirst First Aid Corporation2025-09-08HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47682-397-12Hydrocortisone10 in 1 BOXCREAM1014
47682-397-12Hydrocortisone0.9 g in 1 PACKETCREAM0.914
47682-397-35Hydrocortisone144 in 1 BAGCREAM14414
47682-397-35Hydrocortisone0.9 g in 1 PACKETCREAM0.914
47682-397-71Hydrocortisone0.9 g in 1 PACKETCREAM0.914
47682-397-71Hydrocortisone20 in 1 BOXCREAM2014
47682-397-73Hydrocortisone25 in 1 BOXCREAM2514
47682-397-99Hydrocortisone0.9 g in 1 PACKETCREAM0.914

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47682-397HYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]13Current NDC, Legacy NDC, 8 package rows20240118_69d6645e-db3c-4dc0-a9a5-e2bc963e2f28.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HydrocortisoneACTIVE INGREDIENTWI4X0X7BPJHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
HydrocortisoneACTIVE MOIETYWI4X0X7BPJHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
alcoholINACTIVE INGREDIENT3K9958V90MHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
methylparabenINACTIVE INGREDIENTA2I8C7HI9THYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
mineral oilINACTIVE INGREDIENTT5L8T28FGPHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
paraffinINACTIVE INGREDIENTI9O0E3H2ZEHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
petrolatumINACTIVE INGREDIENT4T6H12BN9UHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
propylparabenINACTIVE INGREDIENTZ8IX2SC1OHHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
waterINACTIVE INGREDIENT059QF0KO0RHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3
white waxINACTIVE INGREDIENT7G1J5DA97FHYDROCORTISONE CREAM [UNIFIRST FIRST AID CORPORATION]3

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 58 of 335 · 6,681 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Blue Star MedicatedCAMPHORFocus Consumer Healthcare, LLC56df008e-a23b-4870-e054-00144ff8d46c2026-04-27WarningsExact identifier
application number: M017
Eagle Brand Muscle RubMENTHOL, METHYL SALICYLATEBorden Company (Private) Limited06cb845c-cc53-1f1d-e063-6394a90a8c012026-04-27WarningsExact identifier
application number: M017
Eagle Brand Medicated Oil AromaticCAMPHOR, MENTHOL, METHYL SALICYLATEPT. EAGLE INDO PHARMA0ef7c3aa-94a3-9fe9-e063-6394a90ab13d2026-04-27WarningsExact identifier
application number: M017
Eagle Brand Medicated OilMENTHOL, METHYL SALICYLATEPT. EAGLE INDO PHARMA5071f145-49f7-0855-e063-6394a90a8f262026-04-27WarningsExact identifier
application number: M017
Eagle Brand Medicated Oil RefreshCAMPHOR, MENTHOLPT. EAGLE INDO PHARMA09260c31-56a3-07aa-e063-6394a90a95fd2026-04-27WarningsExact identifier
application number: M017
Eagle Brand Muscle RubMENTHOL, METHYL SALICYLATEPT. EAGLE INDO PHARMA5072ad57-9fa7-ddba-e063-6394a90a319b2026-04-27WarningsExact identifier
application number: M017
Scriptsusa Hand SanitizerALCOHOLEnergized Solution Corp4f97edd9-717a-315b-e063-6394a90aade72026-04-27WarningsExact identifier
unii: 3K9958V90M
Eagle Brand Medicated Roll On RefreshCAMPHOR, MENTHOLPT. EAGLE INDO PHARMA09235f26-2262-6ca2-e063-6394a90ad8f12026-04-27WarningsExact identifier
application number: M017
Eagle Brand Medicated Roll On AromaticCAMPHOR, MENTHOL, METHYL SALICYLATEPT. EAGLE INDO PHARMA0f333f93-bec6-72d5-e063-6394a90a4e3f2026-04-27WarningsExact identifier
application number: M017
Alcohol wet wipesALCOHOL WET WIPESShandong Aishule Hygiene Products Co., Ltdf79dbac0-cec0-46bc-e053-6294a90a2b132026-04-25WarningsExact identifier
unii: 3K9958V90M
Wet wipesWET WIPESJINGXIN GROUP (M) SDN BHD395225b1-486b-1867-e063-6394a90a18652026-04-25WarningsExact identifier
unii: 3K9958V90M
Hand SanitizerALCOHOLMerchSource, LLC5054a055-50d0-f12a-e063-6294a90ad78e2026-04-25WarningsExact identifier
unii: 3K9958V90M
HIP PAIN RELIEF ROLL-ONLIDOCAINE AND MENTHOLGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.502f1f9e-8552-ca7b-e063-6394a90a7c532026-04-24WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONESportpharm LLCef9cf62a-5805-48bc-915e-c0e91a10837e2026-04-24Adverse reactionsExact identifier
unii: WI4X0X7BPJ
HydrocortisoneHYDROCORTISONESportpharm LLC78f43570-b6fd-42eb-bb9e-580abf79bf0d2026-04-24Adverse reactionsExact identifier
unii: WI4X0X7BPJ
Ethyl AlcoholETHYL ALCOHOLUpLift Brands, LLC5035ec52-2d65-cbbf-e063-6294a90a4a5c2026-04-24Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Foaming Sanitizing HandALCOHOLKutol Products Companyb2e22e51-88f5-4391-8705-3855c1645d802026-04-24WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Amber Breeze ScentedALCOHOLFourstar Group USA, Inc.eb39678d-7576-4147-be02-b7779a5758282026-04-24WarningsExact identifier
unii: 3K9958V90M
B-Pure Moisturizing Hand Sanitizer Kick Off ScentedALCOHOLFourstar Group USA, Inc.860f25c3-54b0-4438-ba97-0fc81cf350442026-04-24WarningsExact identifier
unii: 3K9958V90M
SOMBRA WARM THERAPYMENTHOL CAMPHORSOMBRA COSMETICS INC.de78dba9-53b3-4dbd-9dd2-6a692378da342026-04-24WarningsExact identifier
application number: M017

Reported adverse events (FAERS/openFDA)#

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