Home NDC 63083-2067-2 Anti-Flatulence Formula
Product NDC 63083-2067
Requested package NDC 63083-2067-2
11-digit product format 630832067
Labeler code 63083
Product ID 63083-2067_436beb0d-b3e8-4137-9df9-2a48ce5bd423
Type HUMAN OTC DRUG
Nonproprietary name Anti-Flatulence Formula
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance ACHYRANTHES BIDENTATA ROOT; AILANTHUS ALTISSIMA BARK; LINDERA AGGREGATA ROOT; MAGNOLIA DENUDATA FLOWER BUD; RHEUM PALMATUM ROOT
Active strength 3; 3; 3; 3; 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
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…
Additional Listing Data#
Finished product Yes
Brand name base Anti-Flatulence Formula
Brand name suffix 2067
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACHYRANTHES BIDENTATA ROOT 3 [hp_X]/59mL AILANTHUS ALTISSIMA BARK 3 [hp_X]/59mL MAGNOLIA DENUDATA FLOWER BUD 3 [hp_X]/59mL RHEUM PALMATUM ROOT 3 [hp_X]/59mL LINDERA AGGREGATA ROOT 3 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 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 C67 2026-01-08 C67 2024-01-30 C67 2024-01-30 C67
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2067-2 Anti-Flatulence Formula2067 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 63083-2067 ANTI-FLATULENCE FORMULA 2067 (ANTI-FLATULENCE FORMULA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_25826eed-2def-40f5-86e1-dba6f6ed9b04.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 63083-2067-2 63083206702 59 mL in 1 BOTTLE, DROPPER (63083-2067-2) 59 ml 1985-08-15 0000-00-00 No No Current