Icy Hot Advanced Relief
- Product NDC
- 41167-0805
- 11-digit product format
- 411670805
- Labeler code
- 41167
- Product ID
- 41167-0805_06448d78-4da1-44d6-b327-ea5983e3b548
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol Topical Analgesic
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Chattem, Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-12-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 210 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 41167-0805 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 41167-0805 | 41167-0805-0 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 41167-0805 | 41167-0805-1 | D | Discontinued by firm | 2026-10-05 |
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.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 41167-0805-1 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 41167-0805-0 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 41167-0805-1 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 41167-0805-0 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 41167-0805-0 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 41167-0805-0 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 41167-0805-0 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 41167-0805-0 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 41167-0805-0 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 41167-0805-0 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 41167-0805-0 | 0efc9e666f02… | f202fb6c5f17… |
| 2024-11-09 02:27 UTC · source 2024-11-08 | excluded package | package | 41167-0805-0 | ad56d346431e… | cc804d4bbf1e… |
| 2024-10-04 04:10 UTC · source 2024-10-03 | excluded package | package | 41167-0805-0 | 367a005e9d99… | 383a685ebd0f… |
| 2024-07-10 04:00 UTC · source 2024-07-09 | excluded package | package | 41167-0805-0 | 557ba5c1ecfa… | 9c80585c8c6e… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 41167-0805-0 | EA - Each | 41167-0805 | ed59d252-209f-49ec-b881-927fbe90be31 | 1 | 2021-08-05 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MENTHOL | ACTIVE INGREDIENT | L7T10EIP3A | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 1 | |
| MENTHOL | ACTIVE MOIETY | L7T10EIP3A | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 1 | |
| HYDRATED SILICA | INACTIVE INGREDIENT | Y6O7T4G8P9 | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 1 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 1 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 1 | |
| POLYISOBUTYLENE (1000 MW) | INACTIVE INGREDIENT | 5XB3A63Y52 | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 41167-0805 | ICY HOT ADVANCED RELIEF (MENTHOL TOPICAL ANALGESIC) PATCH [CHATTEM, INC.] | 7 | Legacy NDC | 20241102_1a100d2a-b0b1-47a2-a1df-5cc394a38b84.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41167-0805-1 | 41167080501 | 5 PATCH in 1 CARTON (41167-0805-1) | 5 patch | 2013-10-22 | 0000-00-00 | No | No | Current |