Home NDC 51096-0001 Gluten Sensitivity Formula
Product NDC 51096-0001
11-digit product format 510960001
Labeler code 51096
Product ID 51096-0001_04a36afe-0f09-47fe-8d8d-ad77bf658ee4
Type HUMAN OTC DRUG
Nonproprietary name Lycopodium Clavatum, Pulsatilla
Dosage form CAPSULE
Route ORAL
Labeler The Wise Alternative
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2013-03-01
Marketing end 2029-08-30
Substance LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS
Active strength 12; 12 [hp_X]/mg; [hp_X]/mg
NDC exclude flag No
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 · 42 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 51096-0001-1 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 51096-0001-1 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 51096-0001-1 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 51096-0001-1 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 51096-0001-1 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 51096-0001-1 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 51096-0001-1 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 51096-0001-1 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 51096-0001-1 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 51096-0001-1 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 51096-0001-1 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 51096-0001-1 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 51096-0001-1 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 51096-0001-1 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 51096-0001-1 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51096-0001-1 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 51096-0001-1 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 51096-0001-1 bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 51096-0001-1 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 51096-0001-1 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 51096-0001-1 9bebd1f3094a…5416666fcb17…
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 Gluten Sensitivity Formula Active Ingredients# Ingredient, Strength table Ingredient Strength LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mg PULSATILLA VULGARIS 12 [hp_X]/mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C88X29Y479 Internal UNII lookup I76KB35JEV Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 51096-0001-1 Gluten Sensitivity Formula 180 mg in 1 BOTTLE CAPSULE 180 1
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded LYCOPODIUM CLAVATUM SPORE ACTIVE INGREDIENT C88X29Y479 GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 PULSATILLA VULGARIS ACTIVE INGREDIENT I76KB35JEV GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 LYCOPODIUM CLAVATUM SPORE ACTIVE MOIETY C88X29Y479 GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 PULSATILLA VULGARIS ACTIVE MOIETY I76KB35JEV GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 ARONIA MELANOCARPA FRUIT INACTIVE INGREDIENT S935718Z2Q GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 BROWN RICE INACTIVE INGREDIENT 659G217HPG GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 CARNOSINE INACTIVE INGREDIENT 8HO6PVN24W GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 CHOLECALCIFEROL INACTIVE INGREDIENT 1C6V77QF41 GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 CYBERLINDNERA JADINII RNA INACTIVE INGREDIENT 5620EH64M4 GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 FOLIC ACID INACTIVE INGREDIENT 935E97BOY8 GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 GELATIN INACTIVE INGREDIENT 2G86QN327L GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 ONCORHYNCHUS MASOU SPERM DNA INACTIVE INGREDIENT 1SI16O1B9R GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51096-0001 GLUTEN SENSITIVITY FORMULA (LYCOPODIUM CLAVATUM, PULSATILLA) CAPSULE [THE WISE ALTERNATIVE] 1 Current NDC, Legacy NDC, 1 package rows 20130806_42b2d54a-5e02-44ed-8172-a45c5addf7c2.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 51096-0001-1 51096000101 180 mg in 1 BOTTLE (51096-0001-1) 180 mg 2013-03-01 2029-08-30 No No Historical