Home NDC 65121-887-02 Pain Away Solution
Product NDC 65121-887
Requested package NDC 65121-887-02
11-digit product format 651210887
Labeler code 65121
Product ID 65121-887_579b1f76-1298-684f-e053-2a91aa0a83d7
Type HUMAN OTC DRUG
Nonproprietary name Aconitum Nepellus Hypericum Peforatum Lycopodium Clavatum Phosphorus Rhus Toxicodendron Secale Cornutum
Dosage form SPRAY
Route TOPICAL
Labeler Pure Source, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-08-25
Marketing end 0000-00-00
Substance HYPERICUM PERFORATUM; LYCOPODIUM CLAVATUM SPORE; ACONITUM NAPELLUS; PHOSPHORUS; TOXICODENDRON PUBESCENS LEAF; CLAVICEPS PURPUREA SCLEROTIUM
Active strength 24 [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL; [hp_X]/100mL
NDC exclude flag No
Listing certified through 2020-12-31
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65121-887-01 Pain Away Solution 10 mL in 1 BOTTLE, GLASS SPRAY 10 1 65121-887-02 Pain Away Solution 15 mL in 1 BOTTLE, GLASS SPRAY 15 1 65121-887-03 Pain Away Solution 15 mL in 1 BOTTLE, SPRAY SPRAY 15 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65121-887 PAIN AWAY SOLUTION (ACONITUM NEPELLUS HYPERICUM PEFORATUM LYCOPODIUM CLAVATUM PHOSPHORUS RHUS TOXICODENDRON SECALE CORNUTUM) SPRAY [PURE SOURCE, LLC] 1 Legacy NDC, 3 package rows 20170826_579b1f76-1297-684f-e053-2a91aa0a83d7.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 65121-887-02 65121088702 15 mL in 1 BOTTLE, GLASS (65121-887-02) 15 ml 2017-08-25 0000-00-00 No No Current