Home NDC 53499-9339 Alpha CF
Product NDC 53499-9339
11-digit product format 534999339
Labeler code 53499
Product ID 53499-9339_0f543c7a-ab9b-47f9-beeb-dde04e362379
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
Labeler Schwabe North America, Inc.
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 53499-9339-1 Alpha CF 4 in 1 BOX TABLET 4 9 53499-9339-1 Alpha CF 10 in 1 BLISTER PACK TABLET 10 9 53499-9339-2 Alpha CF 120 in 1 BOTTLE, GLASS TABLET 120 9 53499-9339-2 Alpha CF 1 in 1 BOX TABLET 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53499-9339 ALPHA CF (ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS,) TABLET [SCHWABE NORTH AMERICA, INC.] 9 Current NDC, Legacy NDC, 4 package rows 20220504_ea0e6d54-1a25-4300-8cea-0f7c56afded1.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 North America, Inc. ea0e6d54-1a25-4300-8cea-0f7c56afded1 2022-05-03 Warnings Exact identifier ndc (product): 53499-9339
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 53499-9339-1 53499933901 4 in 1 BOX Historical 53499-9339-2 53499933902 1 BOTTLE, GLASS in 1 BOX (53499-9339-2) / 120 TABLET in 1 BOTTLE, GLASS 2017-04-01 2027-03-31 No No Current