Home NDC 58264-0302-1 A-10
Product NDC 58264-0302
Requested package NDC 58264-0302-1
11-digit product format 582640302
Labeler code 58264
Product ID 58264-0302_2b4df692-11f1-153c-e063-6294a90abc32
Type HUMAN OTC DRUG
Nonproprietary name QUERCUS RUBRA WHOLE, QUERCUS VELUTINA WHOLE, QUERCUS ALBA WOOD, QUERCUS KELLOGGII WHOLE, QUERCUS AGRIFOLIA WHOLE, and QUERCUS GARRYANA WHOLE
Dosage form SOLUTION
Route SUBLINGUAL
Labeler DNA Labs, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1990-01-01
Substance QUERCUS RUBRA WHOLE; QUERCUS VELUTINA WHOLE; QUERCUS ALBA WOOD; QUERCUS KELLOGGII WHOLE; QUERCUS AGRIFOLIA WHOLE; QUERCUS GARRYANA WHOLE
Active strength 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 · 5 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base A-10
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength QUERCUS RUBRA WHOLE 30 [hp_X]/mL QUERCUS VELUTINA WHOLE 30 [hp_X]/mL QUERCUS ALBA WOOD 30 [hp_X]/mL QUERCUS KELLOGGII WHOLE 30 [hp_X]/mL QUERCUS AGRIFOLIA WHOLE 30 [hp_X]/mL QUERCUS GARRYANA WHOLE 30 [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 58264-0302-1 A-10 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 58264-0302 A-10 (QUERCUS RUBRA WHOLE, QUERCUS VELUTINA WHOLE, QUERCUS ALBA WOOD, QUERCUS KELLOGGII WHOLE, QUERCUS AGRIFOLIA WHOLE, AND QUERCUS GARRYANA WHOLE) SOLUTION [DNA LABS, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20250112_136b0cf9-3725-41c0-9f81-65ca5cc48abe.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 A-10 QUERCUS RUBRA WHOLE, QUERCUS VELUTINA WHOLE, QUERCUS ALBA WOOD, QUERCUS KELLOGGII WHOLE, QUERCUS AGRIFOLIA WHOLE, AND QUERCUS GARRYANA WHOLE DNA Labs, Inc. 136b0cf9-3725-41c0-9f81-65ca5cc48abe 2025-01-09 Warnings Exact identifier ndc (package): 58264-0302-1 ndc (product): 58264-0302 ndc11 (package): 58264030201
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 58264-0302-1 58264030201 29.57 mL in 1 BOTTLE, GLASS (58264-0302-1) 29.57 ml 1990-01-01 0000-00-00 No No Current