Home NDC 63083-2109-2 Cold and Flu Formula
Product NDC 63083-2109
Requested package NDC 63083-2109-2
11-digit product format 630832109
Labeler code 63083
Product ID 63083-2109_17d0c8c2-16aa-4658-9a32-b5953f79245c
Type HUMAN OTC DRUG
Nonproprietary name Cold and Flu Formula
Dosage form LIQUID
Route ORAL
Labeler Professional Complementary Health Formulas
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1984-08-15
Substance GINGER; MENTHA PULEGIUM WHOLE; LONICERA HYPOGLAUCA FLOWER; STACHYURUS CHINENSIS WHOLE; FORSYTHIA SUSPENSA FRUIT; ARCTIUM LAPPA FRUIT; ASTRAGALUS PROPINQUUS ROOT; BOS TAURUS PLACENTA
Active strength 2; 3; 3; 3; 3; 3; 6; 6 [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], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
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 Cold and Flu Formula
Brand name suffix 2109
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GINGER 2 [hp_X]/59mL MENTHA PULEGIUM WHOLE 3 [hp_X]/59mL LONICERA HYPOGLAUCA FLOWER 3 [hp_X]/59mL STACHYURUS CHINENSIS WHOLE 3 [hp_X]/59mL FORSYTHIA SUSPENSA FRUIT 3 [hp_X]/59mL ARCTIUM LAPPA FRUIT 3 [hp_X]/59mL ASTRAGALUS PROPINQUUS ROOT 6 [hp_X]/59mL BOS TAURUS PLACENTA 6 [hp_X]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 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 C109 2026-01-08 C109 2024-01-30 C109 2024-01-30 C109
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63083-2109-2 Cold and Flu Formula2109 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 63083-2109 COLD AND FLU FORMULA 2109 (COLD AND FLU FORMULA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] 1 Current NDC, Legacy NDC, 1 package rows 20220216_1f3738ae-00d7-4826-80d3-db3e8b37b089.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 63083-2109-2 63083210902 59 mL in 1 BOTTLE, DROPPER (63083-2109-2) 59 ml 1985-08-15 0000-00-00 No No Current