D-26

Product NDC
58264-0026
11-digit product format
582640026
Labeler code
58264
Product ID
58264-0026_2b9ea85a-20ed-8fa9-e063-6294a90a9ef1
Type
HUMAN OTC DRUG
Nonproprietary name
FERROUS IODIDE, PHOSPHORIC ACID, SULFUR IODIDE, CALCIUM IODIDE, and NITRIC ACID
Dosage form
SOLUTION/ DROPS
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1990-01-01
Substance
CALCIUM IODIDE; FERROUS IODIDE; NITRIC ACID; PHOSPHORIC ACID; SULFUR IODIDE
Active strength
12; 12; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
D-26
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CALCIUM IODIDE12 [hp_X]/mL
FERROUS IODIDE12 [hp_X]/mL
NITRIC ACID12 [hp_X]/mL
PHOSPHORIC ACID12 [hp_X]/mL
SULFUR IODIDE12 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii8EKI9QEE2H, F5452U54PN, 411VRN1TV4, E4GA8884NN, L6L8KA2AA0

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0026-12022-06-02C16284748780-19d75b9d0-2467-f424-e053-dadaa90a57ceD-26
58264-0026-12020-01-31C16284748780-19d75b9d0-2467-f424-e053-dadaa90a57ceD-26

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0026-1D-2629.57 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS29.573

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0026D-26 (FERROUS IODIDE, PHOSPHORIC ACID, SULFUR IODIDE, CALCIUM IODIDE, AND NITRIC ACID) SOLUTION/ DROPS [DNA LABS, INC.]3Current NDC, Legacy NDC, 1 package rows20250115_5ef26695-7b71-4c01-a60c-f72dd1fa342d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58264-0026-15826400260129.57 mL in 1 BOTTLE, GLASS (58264-0026-1) 29.57 ml1990-01-010000-00-00NoNoCurrent