Teevodar Pain Relieving
- Product NDC
- 84483-0001
- 11-digit product format
- 844830001
- Labeler code
- 84483
- Product ID
- 84483-0001_462d75d3-2990-628b-e063-6294a90a99c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Sod-e Biotech Ltd
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-09-01
- Substance
- MENTHOL
- Active strength
- 12.5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 package | package | 84483-0001 | 84483-0001-2 | D | Discontinued by firm | 2026-10-23 |
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
- Teevodar Pain Relieving
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | 12.5 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 416982 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 205b0fef-4f00-db2e-e063-6294a90a93b8 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84483-0001-1 | Teevodar Pain Relieving | 1 in 1 BOX | CREAM | 1 | 2 | |
| 84483-0001-1 | Teevodar Pain Relieving | 50 g in 1 TUBE | CREAM | 50 | 2 | |
| 84483-0001-2 | Teevodar Pain Relieving | 5 g in 1 PACKET | CREAM | 5 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 84483-0001 | TEEVODAR PAIN RELIEVING (MENTHOL) CREAM [SOD-E BIOTECH LTD] | 1 | Current NDC, 3 package rows | 20240901_205b0fef-4f00-db2e-e063-6294a90a93b8.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 |
|---|---|---|---|---|---|---|
| Alocane Max | LIDOCAINE HYDROCHLORIDE AND BENZALKONIUM CHLORIDE | Quest Products LLC | 0a35221a-2fcb-2735-e063-6294a90a88ca | 2025-12-04 | Warnings | M017 |
| Pain Relieving | TROLAMINE SALICYLATE | CARDINAL HEALTH 110, LLC. DBA LEADER | b813262e-57c6-4d2c-8cc0-7a17f6f59343 | 2025-12-04 | Warnings | M017 |
| Gold Bond Medicated Extra Strength Body | MENTHOL | Gold Bond Co LLC | 7b75b7de-9c0b-4edf-b923-320f7d2bb1e6 | 2025-12-04 | Warnings | M017 |
| Lidocaine Patch | LIDOCAINE | Shenzhen Finona Information Technology Co., Ltd | 38767081-7011-6602-e063-6394a90a2784 | 2025-12-03 | Warnings | M017 |
| 4% Lidocaine Maximum Strength Pain Relief | LIDOCAINE | Shenzhen Finona Information Technology Co., Ltd | 3e5a5165-a773-0501-e063-6294a90ae2f4 | 2025-12-03 | Warnings | M017 |
| Leader Lidocaine | LIDOCAINE HCL | CARDINAL HEALTH | cece6765-0e2f-5ce9-e053-2995a90a3758 | 2025-12-03 | Warnings | M017 |
| Westlake Lidocaine | LIDOCAINE HCL | Westlake Pharma LLC | 0c586a14-1a2a-9f42-e063-6294a90a16c1 | 2025-12-03 | Warnings | M017 |
| CVS Lidocaine Maximum Strength | LIDOCAINE HCL | CVS Pharmacy | 87490c0f-a4d9-740e-e053-2a95a90a4724 | 2025-12-03 | Warnings | M017 |
| CVS Maximum Strength Burn | LIDOCAINE HYDROCHLORIDE 4% | CVS Pharmacy | 4510f379-c5a4-92c3-e063-6294a90a0a32 | 2025-12-03 | Warnings | M017 |
| LidoPatch Pain Relief | LIDOCAINE, MENTHOL | JAR Laboratories | 07289aa1-43ed-df31-e063-6394a90a764a | 2025-12-03 | Warnings | M017 |
| Equate Pain Relief Cream | 4% LIDOCAINE HCL | Walmart, Inc | 7d8e8a9a-5474-4c7b-e053-2991aa0a29f5 | 2025-12-03 | Warnings | M017 |
| Solarcaine Burn Pain Relief 4oz | SOLARCAINE BURN PAIN RELIEF 4OZ | WellSpring Pharmaceutical Corporation | 14f23c28-c713-4868-9f46-66363bf94b2c | 2025-12-03 | Warnings | M017 |
| ElixirCortiRelief | HYDROCORTISONE | ELIXIR HEALTHCARE USA, LLC. | a6ca66f3-9759-4c98-a758-45700bc08352 | 2025-12-02 | Warnings | M017 |
| Pain Relief Gel-Patch | LIDOCAINE 4% | Trifecta Pharmaceuticals USA, LLC. | 12a27ce7-c547-7134-e063-6394a90a94bd | 2025-12-02 | Warnings | M017 |
| 5Kind DMSO | MENTHOL, METHYL SALICYLATE | 5KIND TRADING LTD | 6a6c7241-f544-4784-9581-f5b172fdbec7 | 2025-12-02 | Warnings | M017 |
| PEDIADERMICS ECZEMA 2 | HYDROCORTISONE | RENU LABORATORIES, LLC | da840bf6-ed65-bafc-e053-2a95a90a92d5 | 2025-12-02 | Warnings | M017 |
| Thera Plus Maximum Strength Hydrocortisone | HYDROCORTISONE | Fourstar Group USA, Inc | 7d4e21d1-2914-4690-9084-a52abeab0958 | 2025-12-02 | Warnings | M017 |
| Rugby Capsaicin Cream | CAPSAICIN | Rugby Laboratories | 9eca34f1-e91a-3ac1-e053-2a95a90a9bd9 | 2025-12-02 | Warnings | M017 |
| Leader Capsaicin Pain Relief Cream | CAPSAICIN | Cardinal Health 110 dba LEADER | a5620709-0fed-4979-e053-2a95a90ac654 | 2025-12-02 | Warnings | M017 |
| Hydrocortisone Acetate Antipruritic (Anti-Itch) | HYDROCORTISONE ACETATE | Sun Pharmaceutical Industries, Inc. | 9f0b09e7-6cfd-4fd6-8631-67799edf4e08 | 2025-12-02 | Warnings | M017 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 416982 | menthol 1.25 % Topical Cream | PSN | 205b0fef-4f00-db2e-e063-6294a90a93b8 | 2 |
| 416982 | menthol 12.5 MG/ML Topical Cream | SCD | 205b0fef-4f00-db2e-e063-6294a90a93b8 | 2 |
| 416982 | menthol 1.25 % Topical Cream | SY | 205b0fef-4f00-db2e-e063-6294a90a93b8 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 84483-0001-1 | 84483000101 | 1 TUBE in 1 BOX (84483-0001-1) / 50 g in 1 TUBE | 1 tube | 2024-09-01 | No | No | Current |
| 84483-0001-2 | 84483000102 | 5 g in 1 PACKET | 5 g | Historical |