Home NDC 73311-005-03 Flurox Flu
Product NDC 73311-005
Requested package NDC 73311-005-03
11-digit product format 733110005
Labeler code 73311
Product ID 73311-005_910b1db9-9cb8-6b19-e053-2a95a90a1964
Type HUMAN OTC DRUG
Nonproprietary name ANAS BARBARIAE, ASTRAGALUS, ECHINACEA ANG, HYDRASTIS, TAUROXICUM, ZINC PHOS
Dosage form LIQUID
Route ORAL
Labeler CureImmune Corp.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-02
Marketing end 0000-00-00
Substance ASTRAGALUS NUTTALLII LEAF; GOLDENSEAL; ZINC CARBOBENZOXY-.BETA.-ALANYLTAURINATE; ECHINACEA ANGUSTIFOLIA; ZINC PHOSPHATE; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
Active strength 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_M]/1
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record
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 · 18 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…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 73311-005-03 Flurox Flu 1 in 1 BAG LIQUID 1 1 73311-005-03 Flurox Flu 1 in 1 BOTTLE, SPRAY LIQUID 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73311-005 FLUROX FLU (ANAS BARBARIAE, ASTRAGALUS, ECHINACEA ANG, HYDRASTIS, TAUROXICUM, ZINC PHOS) LIQUID [CUREIMMUNE CORP.] 1 Legacy NDC, 2 package rows 20190827_910b0237-94e7-db5a-e053-2a95a90ad703.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 73311-005-03 73311000503 1 BOTTLE, SPRAY in 1 BAG (73311-005-03) > 1 LIQUID in 1 BOTTLE, SPRAY 2015-01-02 0000-00-00 No No Current