Home NDC 68466-3398 ALPHA CF
Product NDC 68466-3398
11-digit product format 684663398
Labeler code 68466
Product ID 68466-3398_508e09f9-a43d-4cd5-9896-9c4eea845c8f
Type HUMAN OTC DRUG
Nonproprietary name ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS
Dosage form TABLET
Route SUBLINGUAL; SUBLINGUAL; SUBLINGUAL
Labeler Schwabe Mexico, S.A. de C.V.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-04-01
Marketing end 2027-03-31
Substance ACONITUM NAPELLUS; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; EUCALYPTUS GLOBULUS LEAF; PHOSPHORUS
Active strength 4; 4; 6; 4; 3; 2; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag No
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 · 12 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…
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 ALPHA CF Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS 4 [hp_X]/1 BRYONIA ALBA ROOT 4 [hp_X]/1 EUPATORIUM PERFOLIATUM FLOWERING TOP 6 [hp_X]/1 GELSEMIUM SEMPERVIRENS ROOT 4 [hp_X]/1 IPECAC 3 [hp_X]/1 EUCALYPTUS GLOBULUS LEAF 2 [hp_X]/1 PHOSPHORUS 6 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 7 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68466-3398-1 ALPHA CF 1 in 1 BOX TABLET 1 7 68466-3398-1 ALPHA CF 120 in 1 BOTTLE, GLASS TABLET 120 7 68466-3398-4 ALPHA CF 4 in 1 BOX TABLET 4 7 68466-3398-4 ALPHA CF 10 in 1 BLISTER PACK TABLET 10 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68466-3398 ALPHA CF (ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS) TABLET [SCHWABE MEXICO, S.A. DE C.V.] 7 Current NDC, Legacy NDC, 4 package rows 20220504_26afa426-eaae-437f-85a7-3bf0ad3d361b.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 ALPHA CF ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS Schwabe Mexico, S.A. de C.V. 26afa426-eaae-437f-85a7-3bf0ad3d361b 2022-05-03 Warnings Exact identifier ndc (product): 68466-3398
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 68466-3398-1 68466339801 1 BOTTLE, GLASS in 1 BOX (68466-3398-1) / 120 TABLET in 1 BOTTLE, GLASS 2017-04-01 2027-03-31 No No Current 68466-3398-4 68466339804 4 in 1 BOX Historical