Home NDC 69676-0028-1 Genexa Motion Sickness Relief
Product NDC 69676-0028
Requested package NDC 69676-0028-1
11-digit product format 696760028
Labeler code 69676
Product ID 69676-0028_d1278653-5240-7f70-e053-2a95a90ab330
Type HUMAN OTC DRUG
Nonproprietary name Bryonia alba, Cinnamonum, Cocculus indica, Colchicum autumnale, Iris versicolor, Kali carbonicum, Nux moschata, Staphysagria, Tabacum, Zingiber officinale
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Genexa Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-01-21
Marketing end 0000-00-00
Substance BRYONIA ALBA WHOLE; CINNAMON; ANAMIRTA COCCULUS SEED; COLCHICUM AUTUMNALE BULB; IRIS VERSICOLOR ROOT; POTASSIUM CARBONATE; NUTMEG; DELPHINIUM STAPHISAGRIA SEED; TOBACCO LEAF; GINGER
Active strength 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [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
Listing certified through 2022-12-31
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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 69676-0028-1 Genexa Motion Sickness Relief 60 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 60 6 69676-0028-1 Genexa Motion Sickness Relief 1 in 1 CARTON TABLET, CHEWABLE 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69676-0028 GENEXA MOTION SICKNESS RELIEF (BRYONIA ALBA, CINNAMONUM, COCCULUS INDICA, COLCHICUM AUTUMNALE, IRIS VERSICOLOR, KALI CARBONICUM, NUX MOSCHATA, STAPHYSAGRIA, TABACUM, ZINGIBER OFFICINALE) TABLET, CHEWABLE [GENEXA INC.] 6 Legacy NDC, 2 package rows 20230121_9bf2a1d6-8a8f-5737-e053-2a95a90a3d99.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69676-0028-1 69676002801 1 BOTTLE, PLASTIC in 1 CARTON (69676-0028-1) > 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC 2020-01-21 0000-00-00 No No Current