Hot and Cold Medicated Patch

Product NDC: 72036-952
11-digit product format: 720360952
Labeler code: 72036
Product ID: 72036-952_47220aa4-f47b-e4c3-e063-6294a90a4e58
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: PATCH
Route: TOPICAL
Labeler: Harris Teeter
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-05-01
Substance: MENTHOL
Active strength: 5 g/100g
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 · 8 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
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	72036-952-05	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	72036-952-05	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	72036-952-05	`bd6a592717d7…`	`303034d00443…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	72036-952-05	`9bebd1f3094a…`	`5416666fcb17…`

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: Hot and Cold Medicated Patch
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	5 g/100g

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
420222	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
9debd4ef-c21b-41ae-afd1-58f47c51c99c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2022-12-08	Hot and Cold Medicated Patch
2022-01-28	Hot and Cold Medicated Patch
2020-07-16	Hot and Cold Medicated Patch
2020-01-31	Hot and Cold Medicated Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72036-952-05	Hot and Cold Medicated Patch	5 in 1 BOX	PATCH	5		5
72036-952-05	Hot and Cold Medicated Patch	9 g in 1 POUCH	PATCH	9		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72036-952	HOT AND COLD MEDICATED PATCH (MENTHOL) PATCH [HARRIS TEETER]	4	Current NDC, Legacy NDC, 2 package rows	20241220_9debd4ef-c21b-41ae-afd1-58f47c51c99c.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 109 of 153 · 3,057 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DCH Pain Relief	LIDOCAINE HCL 4%	Derma Care Research Labs, LLC	00dd70f3-ecc3-33ba-e063-6294a90a4f32	2024-12-19	Warnings	Exact identifier application number: M017
Walgreens Kinesiology Pain Relief	LIDOCAINE, MENTHOL	Walgreen Co.	0fdbb310-8e65-4e0c-b413-a093964324a2	2024-12-19	Warnings	Exact identifier application number: M017
Signature Care Medicated Cold and Hot Patch	MENTHOL	Safeway	0335f1b3-5c8a-67b8-e063-6294a90a9847	2024-12-19	Warnings	Exact identifier application number: M017
HealthWise 4% Lidocaine Cream	LIDOCAINE HYDROCHLORIDE	Veridian Healthcare	0fb2af30-7f2d-c7c4-e063-6294a90a37f7	2024-12-19	Warnings	Exact identifier application number: M017
CVS Health Lidocaine Pain Relief	LIDOCAINE HCL	CVS Pharmacy	445b0778-7266-4e72-97cc-e9e0d0066b61	2024-12-18	Warnings	Exact identifier application number: M017
Dr. Scholls Blister Pain Relief Complete	LIDOCAINE	Scholl's Wellness Company LLC	26e3a678-b28f-588b-e063-6394a90ac025	2024-12-18	Warnings	Exact identifier application number: M017
Dr. Scholls Blister Pain Relief Complete	LIDOCAINE	Scholl's Wellness Company LLC	d860b339-48a0-405c-a67d-f7e7a31f6351	2024-12-18	Warnings	Exact identifier application number: M017
TheraCare Pain Relief Lidocaine	LIDOCAINE	Veridian Healthcare	cea6cdab-28a5-5bd0-e053-2a95a90a1295	2024-12-18	Warnings	Exact identifier application number: M017
TheraCare Pain Relief Medicated	LIDOCAINE AND MENTHOL	Veridian Healthcare	0d092461-85fe-acf6-e063-6294a90a5aae	2024-12-18	Warnings	Exact identifier application number: M017
Hydrocortisone 1%	HYDROCORTISONE	Trifecta Pharmaceuticals Usa Llc	9a23c992-2df9-4bef-9409-47805eecfacd	2024-12-18	Warnings	Exact identifier application number: M017
Pain Relieving Patches	CAMPHOR MENTHOL METHYL SALICYTATE	Walgreen Company	13486792-d3d1-4585-beb7-24720b9edaae	2024-12-18	Warnings	Exact identifier application number: M017
Large Pain Relieving	CAMPHOR MENTHOL METHYL SALICYTATE	Walgreen Company	f9ecfff2-3367-415f-bf68-1a8b7dfe84b8	2024-12-18	Warnings	Exact identifier application number: M017
Tecnu Ivy Complete Kit	IVY TREATMENT	Tec Laboratories Inc.	f047af5d-45d8-11ae-e053-2a95a90a2a22	2024-12-18	Warnings	Exact identifier application number: M017
Extra Large Cool and Heat Patch	MENTHOL	Walgreen Company	9fd83f89-0dd0-4f22-9c8e-a353864ea43b	2024-12-18	Warnings	Exact identifier application number: M017
CAPSAICIN HEAT PATCHES PAIN RELIEF	CAPSAICIN	Rite Aid	e5819a56-e06d-cac9-e053-2995a90ac3ce	2024-12-18	Warnings	Exact identifier application number: M017
Capsaicin Cream	CAPSAICIN	Noble OTC LLC	ed1093f6-a0dc-5d0c-e053-2a95a90a458f	2024-12-18	Warnings	Exact identifier application number: M017
Hydrocortisone 1%	HYDROCORTISONE	Trifecta Pharmaceuticals Usa Llc	9ef5a3b2-c36f-162f-e053-2995a90ae2b0	2024-12-18	Warnings	Exact identifier application number: M017
Hydrocortisone 1%	HYDROCORTISONE	Trifecta Pharmaceuticals Usa Llc	c58904b5-ec72-4cf6-e053-2a95a90a2bfc	2024-12-18	Warnings	Exact identifier application number: M017
Hydrocortisone 1%	HYDROCORTISONE	Trifecta Pharmaceuticals Usa Llc	0a5a35be-9e21-18dd-e063-6394a90a097f	2024-12-18	Warnings	Exact identifier application number: M017
Hydrocortisone 1% with healing aloe	HYDROCORTISONE	Trifecta Pharmaceuticals Usa Llc	0d3321fe-1848-4928-a3cc-d33a8d599977	2024-12-18	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
420222	menthol 5 % Medicated Patch	PSN	9debd4ef-c21b-41ae-afd1-58f47c51c99c	5
420222	menthol 0.05 MG/MG Medicated Patch	SCD	9debd4ef-c21b-41ae-afd1-58f47c51c99c	5
420222	menthol 5 % Medicated Patch	SY	9debd4ef-c21b-41ae-afd1-58f47c51c99c	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72036-952-05	72036095205	5 POUCH in 1 BOX (72036-952-05) / 9 g in 1 POUCH	5 pouch	2018-05-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hot and Cold Medicated Patch	Harris Teeter \| Foshan Aqua Gel Biotech Co.,Ltd.	2025-12-29	HUMAN OTC DRUG LABEL	5