FDA.reportPublic FDA data

Lugols Solution

Product NDC
70804-005
11-digit product format
708040005
Labeler code
70804
Product ID
70804-005_96b0cfea-8787-2ec0-e053-2a95a90ad322
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Iodine
Dosage form
SOLUTION
Route
TRANSDERMAL
Labeler
PURTEX INC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-01-27
Marketing end
0000-00-00
Substance
IODINE
Active strength
1 g/5g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70804-005-082021-01-29C16284748780-1ba0f9c33-29ec-a910-e053-dadaa90a0b85Restricted to use by or on the order of a licensed Physician. Keep cap tightly sealed and protect from light

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70804-005-08Lugols Solution1 g in 1 VIALSOLUTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70804-005LUGOLS SOLUTION (IODINE) SOLUTION [PURTEX INC]2Legacy NDC, 1 package rows20191110_406b1c3c-c4a2-5eb3-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70804-005-08708040005081 g in 1 VIAL1 gHistorical