Home NDC 63083-3012-4 Oxy Bee Pollen Liquescence
Product NDC 63083-3012
Requested package NDC 63083-3012-4
11-digit product format 630833012
Labeler code 63083
Product ID 63083-3012_1e7e4c97-92cf-4881-89cf-49e0e752822d
Type HUMAN OTC DRUG
Nonproprietary name Oxy Bee Pollen Liquescence
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance BEE POLLEN; ENGLISH SOLE; DNA-DIRECTED RNA POLYMERASE SUBUNIT BETA (M. TUBERCULOSIS); BITTER ALMOND; FUCUS VESICULOSUS; LAMINARIA JAPONICA; MEDICAGO SATIVA WHOLE; ROYAL JELLY; ZINC; PANTOTHENIC ACID; COMFREY ROOT
Active strength 2; 2; 2; 3; 3; 3; 3; 3; 4; 6; 6 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fish Proteins, Dietary [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
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 · 15 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 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
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 Oxy Bee Pollen Liquescence
Brand name suffix 3012
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BEE POLLEN 2 [hp_X]/118mL ENGLISH SOLE 2 [hp_X]/118mL DNA-DIRECTED RNA POLYMERASE SUBUNIT BETA (M. TUBERCULOSIS) 2 [hp_X]/118mL BITTER ALMOND 3 [hp_X]/118mL FUCUS VESICULOSUS 3 [hp_X]/118mL LAMINARIA JAPONICA 3 [hp_X]/118mL MEDICAGO SATIVA WHOLE 3 [hp_X]/118mL ROYAL JELLY 3 [hp_X]/118mL ZINC 4 [hp_X]/118mL PANTOTHENIC ACID 6 [hp_X]/118mL COMFREY ROOT 6 [hp_X]/118mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 11 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# Effective, Related label table Effective Related label 2026-01-08 T12 2026-01-08 T12 2024-01-30 T12 2024-01-30 T12
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-3012-4 Oxy Bee Pollen Liquescence3012 118 mL in 1 BOTTLE, DROPPER LIQUID 118 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-3012 OXY BEE POLLEN LIQUESCENCE 3012 (OXY BEE POLLEN LIQUESCENCE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220218_2d6cade7-7e1b-4859-b538-9d0ab70cccb8.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63083-3012-4 63083301204 118 mL in 1 BOTTLE, DROPPER (63083-3012-4) 118 ml 1985-08-15 0000-00-00 No No Current