TopCare Pain Relieving Roll-On

Product NDC: 36800-290
11-digit product format: 368000290
Labeler code: 36800
Product ID: 36800-290_d6e69347-6255-4460-97e1-754359314327
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL, UNSPECIFIED FORM
Dosage form: GEL
Route: TOPICAL
Labeler: Topco Associates LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-09-03
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 40 mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	36800-290-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	36800-290-01	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	36800-290-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	36800-290-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	36800-290-01	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	36800-290-01	`1332a3947898…`	`d4bfe170f9cd…`

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: TopCare Pain Relieving Roll-On
Brand name suffix: Topical Analgesic
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	40 mg/mL

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
415974	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
48589893-ca67-471d-88bc-92014295ab9f	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
36800-290-01	2024-11-13	C162847	48780-1	f386c64a-2164-0266-e053-dadaa90a7c1a	TopCare Pain Relieving Roll-On Gel Topical Analgesic
36800-290-01	2023-01-30	C162847	48780-1	f386c64a-2164-0266-e053-dadaa90a7c1a	TopCare Pain Relieving Roll-On Gel Topical Analgesic

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
36800-290-01	TopCare Pain Relieving Roll-OnTopical Analgesic	74 mL in 1 BOTTLE, WITH APPLICATOR	GEL	74		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
36800-290	TOPCARE PAIN RELIEVING ROLL-ON TOPICAL ANALGESIC (MENTHOL, UNSPECIFIED FORM) GEL [TOPCO ASSOCIATES LLC]	3	Current NDC, Legacy NDC, 1 package rows	20241115_48589893-ca67-471d-88bc-92014295ab9f.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 90 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Re-Lieved Lidocaine Patch	LIDOCAINE PATCH 4%	Transfer Technology	37ef02d4-2ff5-cb23-e063-6294a90a68af	2025-06-19	Warnings	Exact identifier application number: M017
Post-Treatment Repair Cream	HYDROCORTISONE	Vi Medical Products Inc.	ab8885a9-0778-28ff-e053-2995a90a2e12	2025-06-19	Warnings	Exact identifier application number: M017
MyDerm	LIDOCAINE	Inspec Solutions LLC.	82d075d1-c92e-2097-e053-2991aa0ab131	2025-06-18	Warnings	Exact identifier application number: M017
Walgreens Extra Small Lidocaine	LIDOCAINE	Walgreen Co.	dc838e47-d234-4ba5-9449-f645e99be923	2025-06-18	Warnings	Exact identifier application number: M017
CLn Body Moisturizer	COLLOIDAL OAT MOISTURIZER	TopMD Skin Care, Inc.	2de3d68d-a540-d456-e063-6394a90a4b57	2025-06-18	Warnings	Exact identifier application number: M017
Aloe UP SPF 30 Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35967b33-bdfb-ee3c-e063-6294a90a75f6	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35b9dcfa-05f3-3d7b-e063-6394a90a18f1	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Mineral	ZINC OXIDE	Aloe International, LLC	35bc3621-f4e4-42d3-e063-6394a90a7aad	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Kids Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35cd16b0-bd81-8f68-e063-6294a90a3d8c	2025-06-18	Warnings	Exact identifier application number: M017
Aloe Up SPF 50 Kids Mineral	ZINC OXIDE	Aloe International, LLC	35cd5542-947d-a042-e063-6394a90a13f8	2025-06-18	Warnings	Exact identifier application number: M017
Relieve Your Pain	MENTHOL	Proximity Capital Partners LLC dba Asutra	c12369dd-8305-edaf-e053-2995a90a0d3d	2025-06-18	Warnings	Exact identifier application number: M017
Melt Pain Away	CAPSAICIN	Proximity Capital Partners LLC dba Asutra	a95a11d7-a2ae-6654-e053-2a95a90a802c	2025-06-18	Warnings	Exact identifier application number: M017
Recovery Roll-On	MENTHOL, CAMPHOR	PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	ebc9630f-6d8b-e4f0-e053-2995a90a0b49	2025-06-18	Warnings	Exact identifier application number: M017
ProCure Hydrocortisone 1%	HYDROCORTISONE	Twin Med LLC	37cdfabc-1fdb-246a-e063-6394a90a008a	2025-06-17	Warnings	Exact identifier application number: M017
ProCure Hydrocortisone 1%	HYDROCORTISONE	Twin Med LLC	37ce6c35-b211-43de-e063-6294a90ab773	2025-06-17	Warnings	Exact identifier application number: M017
Hydrocortisone with Aloe	HYDROCORTISONE CREAM 1%	Sun Pharmaceutical Industries, Inc.	312ddc8d-100e-cfac-e063-6294a90acd09	2025-06-16	Warnings	Exact identifier application number: M017
Curist 5% Lidocaine	LIDOCAINE 5%	Little Pharma, Inc.	f20241a2-c5b1-f124-e053-2995a90a891b	2025-06-16	Warnings	Exact identifier application number: M017
Toast Screamin Menthol	MENTHOL	IDEAZ, LLC	37b48b1a-ef3d-afdc-e063-6294a90a6610	2025-06-16	Warnings	Exact identifier application number: M017
Toast Freezin Cold	MENTHOL, METHYL SALICYLATE	IDEAZ, LLC	37b4d363-0099-8cd3-e063-6394a90a18d6	2025-06-16	Warnings	Exact identifier application number: M017
Earths Care Anti-Itch	CAMPHOR (NATURAL) AND MENTHOL, UNSPECIFIED FORM	DLC Laboratories, Inc.	ba65f58a-d590-498a-b8e7-a3d78935d880	2025-06-13	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
415974	menthol 4 % Topical Gel	PSN	48589893-ca67-471d-88bc-92014295ab9f	4
415974	menthol 0.04 MG/MG Topical Gel	SCD	48589893-ca67-471d-88bc-92014295ab9f	4
415974	menthol 4 % Topical Gel	SY	48589893-ca67-471d-88bc-92014295ab9f	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
36800-290-01	36800029001	74 mL in 1 BOTTLE, WITH APPLICATOR (36800-290-01)	74 ml	2020-09-03	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
TopCare Pain Relieving Roll-On Gel Topical Analgesic	Topco Associates LLC \| Garcoa, Inc. \| SV Labs Toronto Corporation	2024-11-13	HUMAN OTC DRUG LABEL	4