Home NDC 58264-0353 AM-14
Product NDC 58264-0353
11-digit product format 582640353
Labeler code 58264
Product ID 58264-0353_2b530979-bfa9-24b5-e063-6394a90a76eb
Type HUMAN OTC DRUG
Nonproprietary name SILVER, CALCIUM IODIDE, LYTTA VESICATORIA, COPPER, FERROUS IODIDE, GOLDENSEAL, IODINE, DAPHNE MEZEREUM BARK, PHOSPHORIC ACID, Phosphorus, TOXICODENDRON PUBESCENS LEAF, and RUMEX CRISPUS WHOLE
Dosage form SOLUTION
Route SUBLINGUAL
Labeler DNA Labs, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1990-01-01
Substance CALCIUM IODIDE; COPPER; DAPHNE MEZEREUM BARK; FERROUS IODIDE; GOLDENSEAL; IODINE; LYTTA VESICATORIA; PHOSPHORIC ACID; PHOSPHORUS; RUMEX CRISPUS WHOLE; SILVER; TOXICODENDRON PUBESCENS LEAF
Active strength 8; 12; 30; 8; 6; 6; 6; 6; 30; 6; 12; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Coagulation Factor Activity [PE], Inhibit Ovum Fertilization [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
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 · 10 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 58264-0353-1 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 58264-0353-1 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 58264-0353-1 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 58264-0353-1 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 58264-0353-1 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base AM-14
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SILVER 8 [hp_X]/mL CALCIUM IODIDE 12 [hp_X]/mL LYTTA VESICATORIA 30 [hp_X]/mL COPPER 8 [hp_X]/mL FERROUS IODIDE 6 [hp_X]/mL GOLDENSEAL 6 [hp_X]/mL IODINE 6 [hp_X]/mL DAPHNE MEZEREUM BARK 6 [hp_X]/mL PHOSPHORIC ACID 30 [hp_X]/mL PHOSPHORUS 6 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL RUMEX CRISPUS WHOLE 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 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 58264-0353-1 AM-14 29.57 mL in 1 BOTTLE, GLASS SOLUTION 29.57 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58264-0353 AM-14 (SILVER, CALCIUM IODIDE, LYTTA VESICATORIA, COPPER, FERROUS IODIDE, GOLDENSEAL, IODINE, DAPHNE MEZEREUM BARK, PHOSPHORIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, AND RUMEX CRISPUS WHOLE) SOLUTION [DNA LABS, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20250112_8bf2fde6-fd71-47f8-b5ec-c5e34857ab64.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 AM-14 SILVER, CALCIUM IODIDE, LYTTA VESICATORIA, COPPER, FERROUS IODIDE, GOLDENSEAL, IODINE, DAPHNE MEZEREUM BARK, PHOSPHORIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF, AND RUMEX CRISPUS WHOLE DNA Labs, Inc. 8bf2fde6-fd71-47f8-b5ec-c5e34857ab64 2025-01-09 Warnings Exact identifier ndc (product): 58264-0353
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 58264-0353-1 58264035301 29.57 mL in 1 BOTTLE, GLASS (58264-0353-1) 29.57 ml 1990-01-01 0000-00-00 No No Current