FDA.reportPublic FDA data

Hydrocortisone

Product NDC
71399-0180
11-digit product format
713990180
Labeler code
71399
Product ID
71399-0180_471bfbb4-6df8-9a38-e063-6394a90af1c8
Type
HUMAN OTC DRUG
Nonproprietary name
Hydrocortisone
Dosage form
CREAM
Route
TOPICAL
Labeler
AKRON PHARMA INC
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-06
Substance
HYDROCORTISONE
Active strength
1 mg/100g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Hydrocortisone
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HYDROCORTISONE1 mg/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWI4X0X7BPJ

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
15bd4439-874a-4934-9954-248e5455d460Product name120260310
9962b773-9f2e-22cc-0032-535e48ac417bProduct name320250724
56bb0587-1bf2-48b2-9d93-fc9f59d1eeb2Product name120250325
4d56e8eb-d741-d4a5-de3f-2bab1af75a60Product name720220608
626d7260-31b5-4412-84fd-579746adb6b3Product name120210513
8a011600-5e61-4c59-ab7b-54ab658a3b71Product name220181127
a919621a-248d-3c7a-1084-9f9ce286fdfdProduct name220181009
e7d5a174-836b-a0af-b014-cb0826c69ddcProduct name220181004
fcce390d-6460-4701-87cf-940d8800a1c3Product name220180212
bf065fa6-1e3b-e4c3-0bde-2dc842ceeea1Product name220150218
02657a3f-1489-66ea-f740-5ab9524e57d7Product name120140508
26f3d783-2cc1-4327-e77d-71804cf675a2Product name120140508
36fdc54c-bbeb-981e-8a53-4d768e283892Product name120140508
58f3f9b7-3b9b-a9c1-1c9f-18ac777192b8Product name120140508
61e59a42-186b-9f4b-aec3-fb49a6debc31Product name120140508
705740e1-dee5-2610-c5a3-4c59cd9d62afProduct name120140508
7bdc4804-3832-c0df-e519-72b6d47c9792Product name120140508
a7051cba-790b-a699-81f8-dbbbdbd9b5acProduct name120140508
abaf203f-619e-f265-559f-8c81af5cb1c2Product name120140508
acc4d8bb-0e29-e9f8-65f8-31e94184a9c0Product name120140508
b045ad64-0f28-9a02-2f9b-b34d94fb2278Product name120140508
bfd28ffb-d550-3fe9-f65b-10bcb7f971fdProduct name120140508
da108d9e-edc8-17a3-8c28-3251c6a8acccProduct name120140508
fe21f3fd-a378-0654-1972-db3c3b64470eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71399-0180-12023-03-26C16284748780-1f386c649-b1db-0266-e053-dadaa90a7c1aMEDPURA Hydrocortisone Anti-Itch Cream 1% Maximum Strength with ALOE Drug Facts
71399-0180-12023-01-30C16284748780-1f386c649-b1db-0266-e053-dadaa90a7c1aMEDPURA Hydrocortisone Anti-Itch Cream 1% Maximum Strength with ALOE Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71399-0180-1Hydrocortisone454 g in 1 JARCREAM4547
71399-0180-2Hydrocortisone28 g in 1 TUBECREAM287
71399-0180-2Hydrocortisone1 in 1 CARTONCREAM17

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71399-0180-1GM - Gram71399-0180c273a111-1a9c-4f03-a2bd-9edcb8f32f5112022-01-06
71399-0180-2GM - Gram71399-018024e99158-b799-494e-a000-73fac2e3f3c612025-07-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71399-0180HYDROCORTISONE CREAM [AKRON PHARMA INC]6Current NDC, Legacy NDC, 3 package rows20250120_fa956b6a-1712-4f7a-9490-11866dcd17c8.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71399-0180-171399018001454 g in 1 JAR (71399-0180-1) 454 g2025-01-060000-00-00NoNoCurrent
71399-0180-2713990180021 TUBE in 1 CARTON (71399-0180-2) / 28 g in 1 TUBE1 tube2025-01-06NoNoHistorical