Home NDC 68703-313 NeuropathEase
Product NDC 68703-313
11-digit product format 687030313
Labeler code 68703
Product ID 68703-313_2ab0f647-0253-0e1c-e063-6294a90a74b2
Type HUMAN OTC DRUG
Nonproprietary name Agaricus musc, Arsenicum alb, Hypericum, Phos, Silicea
Dosage form LIQUID
Route ORAL
Labeler Silver Star Brands
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2018-11-19
Substance AMANITA MUSCARIA FRUITING BODY; ARSENIC TRIOXIDE; HYPERICUM PERFORATUM; PHOSPHORUS; SILICON DIOXIDE
Active strength 30; 30; 30; 30; 6 [hp_C]/59mL; [hp_C]/59mL; [hp_C]/59mL; [hp_C]/59mL; [hp_C]/59mL
NDC exclude flag No
Listing certified through 2026-12-31
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 · 8 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 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 68703-313-02 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 68703-313-02 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 68703-313-02 bd6a592717d7…303034d00443…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 68703-313-02 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base NeuropathEase
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMANITA MUSCARIA FRUITING BODY 30 [hp_C]/59mL ARSENIC TRIOXIDE 30 [hp_C]/59mL HYPERICUM PERFORATUM 30 [hp_C]/59mL PHOSPHORUS 30 [hp_C]/59mL SILICON DIOXIDE 6 [hp_C]/59mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
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 68703-313-02 NeuropathEase 59 mL in 1 BOTTLE, DROPPER LIQUID 59 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68703-313 NEUROPATHEASE (AGARICUS MUSC, ARSENICUM ALB, HYPERICUM, PHOS, SILICEA) LIQUID [SILVER STAR BRANDS] 6 Current NDC, Legacy NDC, 1 package rows 20250103_7809e54a-018d-9cf6-e053-2a91aa0aedfe.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 68703-313-02 68703031302 59 mL in 1 BOTTLE, DROPPER (68703-313-02) 59 ml 2018-11-19 0000-00-00 No No Current