Home NDC 58264-0046 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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 58264-0046-1 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 58264-0046-1 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 58264-0046-1 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 58264-0046-1 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 58264-0046-1 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 58264-0046-1 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base D-46
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL LITHIUM CARBONATE 12 [hp_X]/mL SODIUM SULFATE 30 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL RHODODENDRON AUREUM LEAF 6 [hp_X]/mL FILIPENDULA ULMARIA ROOT 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58264-0046-1 D-46 29.57 mL in 1 BOTTLE, GLASS SOLUTION 29.57 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58264-0046 D-46 (FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT) SOLUTION [DNA LABS, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20250115_be8b4acb-83c6-4d25-ba90-ee6e6e0a588e.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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join D-46 FERROSOFERRIC PHOSPHATE, LITHIUM CARBONATE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM LEAF, AND FILIPENDULA ULMARIA ROOT DNA Labs, Inc. be8b4acb-83c6-4d25-ba90-ee6e6e0a588e 2025-01-13 Warnings Exact identifier ndc (product): 58264-0046
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 58264-0046-1 58264004601 29.57 mL in 1 BOTTLE, GLASS (58264-0046-1) 29.57 ml 1990-01-01 0000-00-00 No No Current