D-46

Product NDC
58264-0046
11-digit product format
582640046
Labeler code
58264
Product ID
58264-0046_2b9eb825-2e82-846c-e063-6394a90a0a7b
Type
HUMAN OTC DRUG
Nonproprietary name
Ferrosoferric phosphate, Lithium carbonate, Sodium sulfate, Strychnos nux-vomica seed, Rhododendron Aureum Leaf, and Filipendula ulmaria root
Dosage form
SOLUTION
Route
SUBLINGUAL
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1990-01-01
Substance
FERROSOFERRIC PHOSPHATE; FILIPENDULA ULMARIA ROOT; LITHIUM CARBONATE; RHODODENDRON AUREUM LEAF; SODIUM SULFATE; STRYCHNOS NUX-VOMICA SEED
Active strength
12; 12; 12; 6; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Mood Stabilizer [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
D-46
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FERROSOFERRIC PHOSPHATE12 [hp_X]/mL
FILIPENDULA ULMARIA ROOT12 [hp_X]/mL
LITHIUM CARBONATE12 [hp_X]/mL
RHODODENDRON AUREUM LEAF6 [hp_X]/mL
SODIUM SULFATE30 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED30 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii91GQH8I5F7, 997724QNDS, 2BMD2GNA4V, IV92NQJ73U, 0YPR65R21J, 269XH13919

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
b3053bb1-353b-4a0b-bca5-28fe7228957cProduct name220250124
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
8ce6e144-236f-b7be-f690-f06e0c8c6bd3Product name220170725
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
f09af6ee-c6dd-d0ce-77ad-93508bcdacedProduct name420161205

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58264-0046-12022-06-02C16284748780-19d75b9d1-027c-f424-e053-dadaa90a57ceD-46
58264-0046-12020-01-31C16284748780-19d75b9d1-027c-f424-e053-dadaa90a57ceD-46

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58264-0046-1D-4629.57 mL in 1 BOTTLE, GLASSSOLUTION29.575

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58264-0046D-46 (FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT) SOLUTION [DNA LABS, INC.]5Current NDC, Legacy NDC, 1 package rows20250115_be8b4acb-83c6-4d25-ba90-ee6e6e0a588e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58264-0046-15826400460129.57 mL in 1 BOTTLE, GLASS (58264-0046-1) 29.57 ml1990-01-010000-00-00NoNoCurrent