Home NDC 30056-004 Elgin Pain Relief
Product NDC 30056-004
11-digit product format 300560004
Labeler code 30056
Product ID 30056-004_2bd77bb8-2200-5994-e063-6394a90aaf77
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form GEL
Route TOPICAL
Labeler Eco-Logics, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-07-11
Substance MENTHOL
Active strength 35 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 · 40 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 30056-004-03 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 30056-004-16 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 30056-004-32 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 30056-004-04 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 30056-004-28 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 30056-004-28 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 30056-004-03 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 30056-004-32 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 30056-004-16 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 30056-004-04 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 30056-004-28 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 30056-004-03 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 30056-004-32 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 30056-004-16 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 30056-004-04 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 30056-004-28 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 30056-004-03 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 30056-004-32 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 30056-004-16 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 30056-004-04 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 30056-004-28 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 30056-004-03 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 30056-004-32 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 30056-004-16 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 30056-004-04 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…
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 Elgin Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 35 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 808955 Internal RxNorm 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 30056-004-28 Elgin Pain Relief 3780 g in 1 JUG GEL 3780 27 30056-004-32 Elgin Pain Relief 877 g in 1 BOTTLE, PUMP GEL 877 27 30056-004-16 Elgin Pain Relief 454 g in 1 BOTTLE, PUMP GEL 454 10 30056-004-03 Elgin Pain Relief 85 g in 1 BOTTLE, PUMP GEL 85 7 30056-004-04 Elgin Pain Relief 113.4 g in 1 TUBE GEL 113.4 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Menthol ACTIVE INGREDIENT L7T10EIP3A ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Menthol ACTIVE MOIETY L7T10EIP3A ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Aloe Vera Leaf INACTIVE INGREDIENT ZY81Z83H0X ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Alpha-Tocopherol INACTIVE INGREDIENT H4N855PNZ1 ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Camphor (Natural) INACTIVE INGREDIENT N20HL7Q941 ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Carbomer Homopolymer Type C INACTIVE INGREDIENT 4Q93RCW27E ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 D&C Yellow No. 10 INACTIVE INGREDIENT 35SW5USQ3G ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 FD&C Blue No. 1 INACTIVE INGREDIENT H3R47K3TBD ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Ilex Paraguariensis Leaf INACTIVE INGREDIENT 1Q953B4O4F ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Isopropyl Alcohol INACTIVE INGREDIENT ND2M416302 ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Methylparaben INACTIVE INGREDIENT A2I8C7HI9T ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Trolamine INACTIVE INGREDIENT 9O3K93S3TK ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17 Water INACTIVE INGREDIENT 059QF0KO0R ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 17
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30056-004 ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 27 Current NDC, Legacy NDC, 2 package rows 20250119_70eda21e-e566-42f4-9a49-b0d3ad000652.zip 30056-004 ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 9 Current NDC, Legacy NDC, 1 package rows 20250119_378d1109-6511-1f63-e054-00144ff88e88.zip 30056-004 ELGIN PAIN RELIEF (MENTHOL) GEL [ECO-LOGICS, INC.] 6 Current NDC, Legacy NDC, 2 package rows 20250119_375bfe83-c895-3ea7-e054-00144ff88e88.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 12 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Natures Willow Balm Roll On Pain Relief MENTHOL WB Ventures LLC 3b1834e6-75cd-5380-e063-6294a90ad1d5 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Balm Itch Relief Cream MENTHOL WB Ventures LLC 0ce31b5d-4401-460c-e063-6394a90ab558 2026-07-08 Warnings Exact identifier application number: M017 CAREALL Hydrocortisone Maximum Strength HYDROCORTISONE New World Imports, Inc. 560a4abf-31dd-333f-e063-6294a90a3505 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Balm MENTHOL WB VENTURES LLC b9f50c43-b0d5-39a8-e053-2995a90a04f1 2026-07-08 Warnings Exact identifier application number: M017 Natures Willow Bug Bite Balm MENTHOL WB Ventures LLC b9fab18f-32c7-d5bd-e053-2995a90a6d0f 2026-07-08 Warnings Exact identifier application number: M017 Salonpas pain relieving hot CAPSAICIN, MENTHOL Hisamitsu Pharmaceutical Co., Inc. d2aa8820-a947-404b-b617-e692fbd16502 2026-07-07 Warnings Exact identifier application number: M017 Quali Yi Tiao Gen Pain Patch CAPSAICIN PATCH Sheng Chang Pharmaceutical Co, Ltd. Zhongli Factory 33154a9b-f6d0-4e95-b4cb-6b938f5dcf4d 2026-07-07 Warnings Exact identifier application number: M017 MUYOHON Numbing Cream NUMBING CREAM Guangzhou Jingliang Cosmetics Co., Ltd. 55caf0a5-f062-a6c3-e063-6294a90ae073 2026-07-04 Warnings Exact identifier application number: M017 Targeted Warming Capsaicin Patch CAPSAICIN Army & Air Force Exchange Service 55b539f8-38c4-594e-e063-6394a90afbaa 2026-07-03 Warnings Exact identifier application number: M017 TopCare Health Pain Relief LIDOCAINE HYDROCHLORIDE Topco Associates LLC 485b0671-da09-19d7-e063-6294a90aca5d 2026-07-03 Warnings Exact identifier application number: M017 Mineral Ice Methol Pain Relief MENTHOL 10.5 % Sunflora Inc 6ddd9e97-f717-4d5a-9658-26449a3cc831 2026-07-02 Warnings Exact identifier application number: M017 Burn Relief LIDOCAINE AmerisourceBergen Drug Corporation 7d898e33-ded7-c9b9-e053-2a91aa0adf7c 2026-07-01 Warnings Exact identifier application number: M017 Desert Harvest Releveum with Lidocaine LIDOCAINE HYDROCHLORIDE Desert Harvest, Inc 9ad514ab-a6bd-4564-8ba3-0149032ebf36 2026-07-01 Warnings Exact identifier application number: M017 CVS No Mess Cortisone HYDROCORTISONE Natural Essentials, Inc. 558c94ec-95f1-eb98-e063-6394a90a1e72 2026-07-01 Warnings Exact identifier application number: M017 MUSCLE EASE MENTHOL CAMPHOR SOMBRA COSMETICS INC. 03fff4bf-04ed-49a6-b40f-4d98c2b42f69 2026-07-01 Warnings Exact identifier application number: M017 OrthoNesic Pain Relieving Gel MENTHOL, CAMPHOR Blaine Labs Inc. 122f60c2-f8df-4625-8bb8-a2244a261b5d 2026-07-01 Warnings Exact identifier application number: M017 Desert Harvest RELEVEUM LIDOCAINE Desert Harvest Inc. 5d9010ec-d482-44ff-ba27-3bfec5a241c6 2026-06-30 Warnings Exact identifier application number: M017 Promescent LIDICAINE Absorption 5b508238-3be7-4b0d-bf35-51de79f58f55 2026-06-30 Warnings Exact identifier application number: M017 Lidovyx LIDOCAINE 4% V2 Pharma LLC 4465eb60-a617-4608-9504-8b3b4c64f49e 2026-06-30 Warnings Exact identifier application number: M017 Dr.Johnes Lidocaine 4% Topical Analgesic Cream LIDOCAINE HCL,MENTHOL Dr.Johnes LLC 6144708d-4b0f-4f0d-88e3-6925ba2d004d 2026-06-29 Warnings Exact identifier application number: M017
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 30056-004-03 30056000403 85 g in 1 BOTTLE, PUMP (30056-004-03) 85 g 2016-07-11 No No Current 30056-004-04 30056000404 113.4 g in 1 TUBE (30056-004-04) 113.4 g 2016-07-11 No No Current 30056-004-16 30056000416 454 g in 1 BOTTLE, PUMP (30056-004-16) 454 g 2016-07-11 No No Current 30056-004-28 30056000428 3780 g in 1 JUG (30056-004-28) 3780 g 2016-07-11 No No Current 30056-004-32 30056000432 877 g in 1 BOTTLE, PUMP (30056-004-32) 877 g 2016-07-11 No No Current