Home NDC 43846-0059-1 Shingles Pain Relief
Product NDC 43846-0059
Requested package NDC 43846-0059-1
11-digit product format 438460059
Labeler code 43846
Product ID 43846-0059_2c6a8c16-b524-4219-90a3-c1e6a1c23bb8
Type HUMAN OTC DRUG
Nonproprietary name Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (Smilax Regelii)
Dosage form LIQUID
Route TOPICAL
Labeler Peaceful Mountain, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2016-03-24
Marketing end 2024-09-04
Substance CALENDULA OFFICINALIS FLOWERING TOP; CROTON TIGLIUM SEED; SODIUM CHLORIDE; PLANTAGO MAJOR; TOXICODENDRON PUBESCENS LEAF; SMILAX ORNATA ROOT
Active strength 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 0000-00-00
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 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43846-0059-1 43846005901 30 mL in 1 BOTTLE, SPRAY (43846-0059-1) 30 ml 2016-03-24 2024-09-04 No No Current