Home NDC 59262-241 Nasal Allergy Relief
Product NDC 59262-241
11-digit product format 592620241
Labeler code 59262
Product ID 59262-241_76f74dfb-319a-488c-bbe4-14cf17200568
Type HUMAN OTC DRUG
Nonproprietary name cardiospermum halicacabum flowering top, galphimia glauca flowering top, luffa operculata fruit and schoenocaulon officinale seed
Dosage form SPRAY
Route NASAL
Labeler Similasan Corporation
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2010-05-15
Marketing end 0000-00-00
Substance CARDIOSPERMUM HALICACABUM FLOWERING TOP; GALPHIMIA GLAUCA FLOWERING TOP; LUFFA OPERCULATA FRUIT; SCHOENOCAULON OFFICINALE SEED
Active strength 6 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL
NDC exclude flag No
Listing certified through 2024-12-31
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 · 22 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 59262-241-20 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 59262-241-20 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 59262-241-20 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 59262-241-20 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 59262-241-20 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 59262-241-20 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 59262-241-20 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 59262-241-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 59262-241-20 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 59262-241-20 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 59262-241-20 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59262-241-20 Nasal Allergy Relief 20 mL in 1 BOTTLE, SPRAY SPRAY 20 10
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded CARDIOSPERMUM HALICACABUM FLOWERING TOP ACTIVE INGREDIENT MZP2508BRR NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 GALPHIMIA GLAUCA FLOWERING TOP ACTIVE INGREDIENT 93PH5Q8M7E NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 LUFFA OPERCULATA FRUIT ACTIVE INGREDIENT C4MO6809HU NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 SCHOENOCAULON OFFICINALE SEED ACTIVE INGREDIENT 6NAF1689IO NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 CARDIOSPERMUM HALICACABUM FLOWERING TOP ACTIVE MOIETY MZP2508BRR NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 GALPHIMIA GLAUCA FLOWERING TOP ACTIVE MOIETY 93PH5Q8M7E NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 LUFFA OPERCULATA FRUIT ACTIVE MOIETY C4MO6809HU NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 SCHOENOCAULON OFFICINALE SEED ACTIVE MOIETY 6NAF1689IO NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8 WATER INACTIVE INGREDIENT 059QF0KO0R NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59262-241 NASAL ALLERGY RELIEF (CARDIOSPERMUM HALICACABUM FLOWERING TOP, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION] 10 Legacy NDC, 1 package rows 20230106_f2cd8411-877b-4a9c-bf6a-17f9c3ea5581.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59262-241-20 59262024120 20 mL in 1 BOTTLE, SPRAY (59262-241-20) 20 ml 2010-05-15 0000-00-00 No No Current