Muscle Rub Pain Reliever Gel
- Product NDC
- 52000-072
- 11-digit product format
- 520000072
- Labeler code
- 52000
- Product ID
- 52000-072_5a5dead1-f041-4e5b-acb4-30ff321647d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, UNSPECIFIED FORM
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Universal Distribution Centre LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-01-24
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 25 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
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 | 52000-072 | I | Inactivated by FDA | 2026-10-23 | ||
| excluded package | package | 52000-072 | 52000-072-02 | I | Inactivated by FDA | 2026-10-23 |
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 | 52000-072-02 | 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 | 52000-072-02 | f5e01cc5f278… | a2eaf40c39c3… |
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
- Muscle Rub Pain Reliever Gel
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL, UNSPECIFIED FORM | 25 mg/g |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52000-072-02 | 2025-07-29 | C162847 | 48780-1 | 3b156c62-308b-fb37-e063-e6dba90a4e07 | Pain Reliever Gel |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 52000-072-01 | Muscle Rub Pain Reliever Gel | 35.4 g in 1 TUBE | GEL | 35.4 | 4 | |
| 52000-072-02 | Muscle Rub Pain Reliever Gel | 1 in 1 CARTON | GEL | 1 | 4 | |
| 52000-072-03 | Muscle Rub Pain Reliever Gel | 35.4 g in 1 TUBE | GEL | 35.4 | 3 | |
| 52000-072-04 | Muscle Rub Pain Reliever Gel | 1 in 1 CARTON | GEL | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 52000-072 | MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241212_b9a563b6-7988-79df-e053-2995a90a752b.zip |
| 52000-072 | MUSCLE RUB PAIN RELIEVER GEL (MENTHOL, UNSPECIFIED FORM) GEL [UNIVERSAL DISTRIBUTION CENTRE LLC] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241218_18536e21-afc3-8447-e063-6394a90aabae.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Biofreeze Roll-On | MENTHOL | A-S Medication Solutions | 814b37ea-5441-4cec-8794-71ca01d849ae | 2023-10-30 | Warnings | M017 |
| Dr. Sheffield Hydrocortisone Anti itch | HYDROCORTISONE | Sheffield Pharmaceuticals LLC | 71c9f2f4-2188-45eb-b55e-3856ac78070b | 2023-10-30 | Warnings | M017 |
| Family Wellness | BENZOCAINE, RESORCINOL | Zhejiang Jingwei Pharmaceutic Al Co., Ltd. | df540eb8-6773-4647-9cc2-c3fd14d7355e | 2023-10-27 | Warnings | M017 |
| Family Wellness | HYDROCORTISONE 1% | FRONT PHARMACEUTICAL PLC | ea26265d-f24e-458e-8bf0-287b2d49f4f4 | 2023-10-27 | Warnings | M017 |
| Joint Formula 88 MAX PLUS | CAMPHOR | Sarati International, Inc. | f5d78335-b78d-4909-a88b-9daa3c18ba15 | 2023-10-27 | Warnings | M017 |
| OsmoFlex | MENTHOL | Sarati International, Inc. | 479147c0-4cf4-4d7a-8b8e-1a0de49ed73e | 2023-10-27 | Warnings | M017 |
| Thera plus Anti-itch with aloe Hydrocortisone | HYDROCORTISONE | Fourstar Group USA, Inc. | c69d0670-a65b-1680-e053-2995a90a2ee5 | 2023-10-26 | Warnings | M017 |
| Family Wellness | DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE | FRONT PHARMACEUTICAL PLC | fde2069b-344e-46da-bb95-c5113e0f35d6 | 2023-10-26 | Warnings | M017 |
| MAXIMUM STRENGTH HEMORRHOIDAL RELIEF | LIDOCAINE | CVS PHARMACY, INC | b61424bf-3b23-420b-a7bc-256ddb96aa22 | 2023-10-25 | Warnings | M017 |
| Assured | HYDROCORTISONE | Zhejiang Jingwei Pharmaceutic Al Co., Ltd. | bc97f364-9443-47b8-9c2d-b5dcc00cc9b7 | 2023-10-25 | Warnings | M017 |
| Stopain Clinical | MENTHOL, UNSPECIFIED FORM | Troy Manufacturing, Inc. | b41091b4-0dc0-4a88-8ff6-11979b3d307a | 2023-10-25 | Warnings | M017 |
| Thera Plus | HYDROCORTISONE | Zhejiang Jingwei Pharmaceutical Co., Ltd. | bcc99e5a-2403-46da-9c9d-8411fa4104e0 | 2023-10-25 | Warnings | M017 |
| Assured | LIDOCAINE HYDROCHLORIDE | Zhejiang Jingwei Pharmaceutical Co., Ltd. | ab25c47d-bbe6-4e2b-9e39-dd9f4da3ee8c | 2023-10-25 | Warnings | M017 |
| Red hot | CAPSAICIN | The Hygenic Company, LLC | d100092c-e10b-2063-e053-2995a90aedb2 | 2023-10-25 | Warnings | M017 |
| Stopain Clinical | MENTHOL | Troy Manufacturing, Inc. | c8d4ae28-efc4-6a00-e053-2a95a90a40bf | 2023-10-25 | Warnings | M017 |
| Cryo10 Topical Analgesic | MENTHOL | Element 26 LLC | ff1d2140-9302-918c-e053-6394a90acb9a | 2023-10-25 | Warnings | M017 |
| Stopain Clinical | MENTHOL | Troy Manufacturing, Inc. | 3336cc35-e773-4705-84b5-61040604beef | 2023-10-25 | Warnings | M017 |
| CARMEX Multi-Symptom 3 in 1 COLD Sore treatment External Analgesic Skin Protectant | BENZOCAINE, WHITE PETROLATUM | Carma Laboratories, Inc. | bbf0abcd-b7d6-b5e4-e053-2995a90a5240 | 2023-10-25 | Warnings | M017 |
| Carmex Classic Lip Balm Medicated | CAMPHOR (SYNTHETIC), WHITE PETROLATUM | Carma Laboratories, Inc. | bbee66b9-39ff-4e7e-e053-2995a90a43be | 2023-10-25 | Warnings | M017 |
| XtraCare Ice Cold Topical Analgesic Gel | MENTHOL | Rejoice International | d38f3099-d940-44d8-aa7f-404157c5e0e3 | 2023-10-24 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 282805 | menthol 2.5 % Topical Gel | PSN | b9a563b6-7988-79df-e053-2995a90a752b | 4 |
| 282805 | menthol 0.025 MG/MG Topical Gel | SCD | b9a563b6-7988-79df-e053-2995a90a752b | 4 |
| 282805 | menthol 2.5 % Topical Gel | SY | b9a563b6-7988-79df-e053-2995a90a752b | 4 |
| 282805 | menthol 2.5 % Topical Gel | PSN | 18536e21-afc3-8447-e063-6394a90aabae | 3 |
| 282805 | menthol 0.025 MG/MG Topical Gel | SCD | 18536e21-afc3-8447-e063-6394a90aabae | 3 |
| 282805 | menthol 2.5 % Topical Gel | SY | 18536e21-afc3-8447-e063-6394a90aabae | 3 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 52000-072-01 | 52000007201 | 35.4 g in 1 TUBE | 35.4 g | Historical | ||||
| 52000-072-02 | 52000007202 | 1 TUBE in 1 CARTON (52000-072-02) > 35.4 g in 1 TUBE (52000-072-01) | 1 tube | 2021-01-24 | 0000-00-00 | No | No | Current |
| 52000-072-03 | 52000007203 | 35.4 g in 1 TUBE | 35.4 g | Historical | ||||
| 52000-072-04 | 52000007204 | 1 TUBE in 1 CARTON (52000-072-04) / 35.4 g in 1 TUBE (52000-072-03) | 1 tube | 2021-01-24 | No | No | Current |