FDA.reportPublic FDA data

Maximum Strength Cortisone

Product NDC
69842-259
11-digit product format
698420259
Labeler code
69842
Product ID
69842-259_48645556-baea-1030-e063-6394a90a2cfa
Type
HUMAN OTC DRUG
Nonproprietary name
Hydrocortisone Ointment
Dosage form
OINTMENT
Route
TOPICAL
Labeler
CVS Pharmacy
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-11-01
Substance
HYDROCORTISONE
Active strength
1 g/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
Maximum Strength Cortisone
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HYDROCORTISONE1 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWI4X0X7BPJ
Rxcui203105

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
69842-259-032024-02-06C16284748780-1f386c64a-0866-0266-e053-dadaa90a7c1aCVS MAXIMUM STRENGTH CORTISONE OINTMENT
69842-259-032023-01-30C16284748780-1f386c64a-0866-0266-e053-dadaa90a7c1aCVS MAXIMUM STRENGTH CORTISONE OINTMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-259-01Maximum Strength Cortisone28 g in 1 TUBEOINTMENT286
69842-259-03Maximum Strength Cortisone1 in 1 CARTONOINTMENT16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-259MAXIMUM STRENGTH CORTISONE (HYDROCORTISONE OINTMENT) OINTMENT [CVS PHARMACY]4Current NDC, Legacy NDC, 2 package rows20241227_f25f2e14-4fc9-4c92-880d-e5f9279d4ecd.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
203105hydrocortisone 1 % Topical OintmentPSNf25f2e14-4fc9-4c92-880d-e5f9279d4ecd6
203105hydrocortisone 0.01 MG/MG Topical OintmentSCDf25f2e14-4fc9-4c92-880d-e5f9279d4ecd6
203105hydrocortisone 1 % Topical OintmentSYf25f2e14-4fc9-4c92-880d-e5f9279d4ecd6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-259-016984202590128 g in 1 TUBE28 gHistorical
69842-259-03698420259031 TUBE in 1 CARTON (69842-259-03) / 28 g in 1 TUBE (69842-259-01) 1 tube2016-11-010000-00-00NoNoCurrent