FDA.reportPublic FDA data

IODIUM

Product NDC
15631-2787
11-digit product format
156312787
Labeler code
15631
Product ID
15631-2787_1a345d76-d7b7-2cfc-e063-6294a90af205
Type
HUMAN OTC DRUG
Nonproprietary name
IODIUM
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-05-23
Substance
IODINE
Active strength
3 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
IODIUM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IODINE3 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9679TC07X4Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1a3471b1-1824-4a08-e063-6294a90ad36dAvailable on FDA.report

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-2787-0IODIUM10 mL in 1 BOTTLELIQUID101
15631-2787-1IODIUM30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-2787IODIUM LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Current NDC, 2 package rows20240607_1a3471b1-1824-4a08-e063-6294a90ad36d.zip

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IODIUMIODIUMRxhomeo Private Limited d.b.a. Rxhomeo, Inc1a3471b1-1824-4a08-e063-6294a90ad36d2024-06-06WarningsExact identifier
ndc (product): 15631-2787

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
15631-2787-01563127870010 mL in 1 BOTTLE (15631-2787-0) 10 ml2024-05-23NoNoCurrent
15631-2787-11563127870130 mL in 1 BOTTLE (15631-2787-1) 30 ml2024-05-23NoNoCurrent