Home NDC 53799-220-42 Itch Relief
Product NDC 53799-220
Requested package NDC 53799-220-42
11-digit product format 537990220
Labeler code 53799
Product ID 53799-220_d4452115-6c33-4fc5-a362-f0f64ee8f13f
Type HUMAN OTC DRUG
Nonproprietary name apis mellifera, lachesis muta venom, ledum palustre twig and urtica urens
Dosage form LIQUID
Route TOPICAL
Labeler Similasan AG
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-04-23
Marketing end 0000-00-00
Substance APIS MELLIFERA; LACHESIS MUTA VENOM; LEDUM PALUSTRE TWIG; URTICA URENS
Active strength 12 [hp_X]/7.5mL; [hp_X]/7.5mL; [hp_X]/7.5mL; [hp_X]/7.5mL
NDC exclude flag No
Listing certified through 2022-12-31
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 · 15 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…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
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 53799-220-42 Itch Relief 7.5 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 7.5 2 53799-220-42 Itch Relief 1 in 1 BOX LIQUID 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53799-220 ITCH RELIEF (APIS MELLIFERA, LACHESIS MUTA VENOM, LEDUM PALUSTRE TWIG AND URTICA URENS) LIQUID [SIMILASAN AG] 2 Legacy NDC, 2 package rows 20210424_9c0ab676-c8a4-4896-b91d-720d280a135d.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 53799-220-42 53799022042 1 BOTTLE, WITH APPLICATOR in 1 BOX (53799-220-42) > 7.5 mL in 1 BOTTLE, WITH APPLICATOR 2021-04-23 0000-00-00 No No Current