FDA.reportPublic FDA data

Cold Bee Gone

Product NDC
70449-1000
Requested package NDC
70449-1000-2
11-digit product format
704491000
Labeler code
70449
Product ID
70449-1000_ece6292a-bef6-d9ac-e053-2995a90af580
Type
HUMAN OTC DRUG
Nonproprietary name
Kali Bichromicum 6X, Sabadilla 6X, Luffa Operculata 6X
Dosage form
LIQUID
Route
NASAL
Labeler
Buzzagogo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-01
Marketing end
0000-00-00
Substance
LUFFA OPERCULATA FRUIT; POTASSIUM DICHROMATE; SCHOENOCAULON OFFICINALE SEED
Active strength
6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage70449-100070449-1000-2IInactivated by FDA2026-10-05

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 · 11 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
70449-1000-12024-07-30Cold Bee Gone
70449-1000-22024-07-30Cold Bee Gone
70449-1000-12024-01-30Cold Bee Gone
70449-1000-22024-01-30Cold Bee Gone
70449-1000-12021-10-06Cold Bee Gone
70449-1000-22021-10-06Cold Bee Gone
70449-1000-12021-01-29Cold Bee Gone
70449-1000-22021-01-29Cold Bee Gone

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70449-1000-1Cold Bee Gone1 in 1 BOXLIQUID15
70449-1000-1Cold Bee Gone10 mL in 1 JARLIQUID105
70449-1000-2Cold Bee Gone10 mL in 1 TUBELIQUID105
70449-1000-2Cold Bee Gone1 in 1 BOXLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70449-1000COLD BEE GONE (KALI BICHROMICUM 6X, SABADILLA 6X, LUFFA OPERCULATA 6X) LIQUID [BUZZAGOGO, INC]5Legacy NDC, 4 package rows20221108_2a581c16-a682-5a75-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70449-1000-2704491000021 TUBE in 1 BOX (70449-1000-2) > 10 mL in 1 TUBE1 tube2017-01-010000-00-00NoNoCurrent