Home NDC 63083-6044-2 Plastics/BPA Detox
Product NDC 63083-6044
Requested package NDC 63083-6044-2
11-digit product format 630836044
Labeler code 63083
Product ID 63083-6044_45c48399-e70f-414e-9479-282f02e6e17b
Type HUMAN OTC DRUG
Nonproprietary name Plastics/BPA Detox
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ARCTIUM LAPPA ROOT OIL; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER; BOS TAURUS BRAIN; BEEF KIDNEY; BEEF LIVER; BOS TAURUS LYMPH VESSEL; BISPHENOL A; METHYL METHACRYLATE; CARBONATE ION; SODIUM POLYSTYRENE SULFONATE; TRIS(2-ETHYLHEXYL)PHOSPHATE
Active strength 3; 3; 3; 6; 6; 6; 6; 12; 12; 12; 12; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Meat Proteins [EXT], 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 Plastics/BPA Detox
Brand name suffix 6044
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARCTIUM LAPPA ROOT OIL 3 [hp_X]/59mL TARAXACUM OFFICINALE 3 [hp_X]/59mL TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/59mL BOS TAURUS BRAIN 6 [hp_X]/59mL BEEF KIDNEY 6 [hp_X]/59mL BEEF LIVER 6 [hp_X]/59mL BOS TAURUS LYMPH VESSEL 6 [hp_X]/59mL BISPHENOL A 12 [hp_X]/59mL METHYL METHACRYLATE 12 [hp_X]/59mL CARBONATE ION 12 [hp_X]/59mL SODIUM POLYSTYRENE SULFONATE 12 [hp_X]/59mL TRIS(2-ETHYLHEXYL)PHOSPHATE 12 [hp_X]/59mL
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# Effective, Related label table Effective Related label 2026-01-08 X44 2026-01-08 X44 2024-01-30 X44 2024-01-30 X44
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-6044-2 Plastics/BPA Detox6044 59 mL in 1 BOTTLE, DROPPER LIQUID 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63083-6044 PLASTICS/BPA DETOX 6044 (PLASTICS/BPA DETOX) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220406_9c57ecd2-c2e0-4e82-ae67-c91b041a2639.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 63083-6044-2 63083604402 59 mL in 1 BOTTLE, DROPPER (63083-6044-2) 59 ml 1985-08-15 0000-00-00 No No Current