Alcortin

Product NDC
68040-702
11-digit product format
680400702
Labeler code
68040
Product ID
68040-702_4acf85e5-f2d5-40b0-8562-2427a2ab56be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
1% iodoquinol - 2% hydrocortisone
Dosage form
GEL
Route
TOPICAL
Labeler
Primus Pharmaceuticals
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2003-07-25
Marketing end
0000-00-00
Substance
HYDROCORTISONE; IODOQUINOL
Active strength
2 g/100g; g/100g
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68040-702-02Alcortin2 g in 1 PACKETGEL23
68040-702-08Alcortin10 in 1 CARTONGEL103
68040-702-08Alcortin64 in 1 BOXGEL643
68040-702-13Alcortin12 in 1 BOXGEL123
68040-702-13Alcortin24 in 1 CARTONGEL243

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68040-702ALCORTIN (1% IODOQUINOL - 2% HYDROCORTISONE) GEL [PRIMUS PHARMACEUTICALS]3Legacy NDC, 5 package rows20100719_995ae132-8e37-4fda-b353-ce79ab9d0bf4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1191414Alcortin 1 % / 2 % Topical GelPSN995ae132-8e37-4fda-b353-ce79ab9d0bf43
544118iodoquinol 1 % / hydrocortisone 2 % Topical GelPSN995ae132-8e37-4fda-b353-ce79ab9d0bf43
1191414hydrocortisone 0.02 MG/MG / iodoquinol 0.01 MG/MG Topical Gel [Alcortin]SBD995ae132-8e37-4fda-b353-ce79ab9d0bf43
544118hydrocortisone 0.02 MG/MG / iodoquinol 0.01 MG/MG Topical GelSCD995ae132-8e37-4fda-b353-ce79ab9d0bf43
1191414Alcortin (hydrocortisone 2 % / iodoquinol 1 % ) Topical GelSY995ae132-8e37-4fda-b353-ce79ab9d0bf43
544118hydrocortisone 2 % / iodoquinol 1 % Topical GelSY995ae132-8e37-4fda-b353-ce79ab9d0bf43

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
68040-702-02680400702022 g in 1 PACKET2 gHistorical
68040-702-086804007020810 in 1 CARTONHistorical
68040-702-136804007021312 in 1 BOXHistorical