SORE NO MORE COOL THERAPY

Product NDC: 61577-3235
11-digit product format: 615773235
Labeler code: 61577
Product ID: 61577-3235_3622f4f5-48bf-9035-e063-6294a90afac2
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: GEL
Route: TOPICAL
Labeler: SOMBRA COSMETICS INC.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-06-14
Substance: MENTHOL
Active strength: .06 g/g
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 2 · 72 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-6	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-7	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-4	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-9	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-1	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-5	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-2	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-3235-8	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-6	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-7	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-4	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-9	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-1	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-5	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-2	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-3235-8	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-6	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-7	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-4	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-9	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-1	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-5	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-2	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-3235-8	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-6	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-7	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-4	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-9	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-1	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-5	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-2	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-3235-8	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-5	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-7	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-6	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-2	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-8	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-9	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-1	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-3235-4	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-5	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-7	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-6	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-2	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-8	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-9	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-1	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-3235-4	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-3235-5	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-3235-7	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-3235-6	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-3235-2	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-3235-8	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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: SORE NO MORE COOL THERAPY
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	.06 g/g

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
415976	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
9aa1f0ac-3baf-4e45-9e3a-c28a99b22909	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
61577-3235-1	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-2	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-4	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-5	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-6	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-7	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-8	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-9	2025-05-27	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-1	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-2	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-4	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-5	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-6	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-7	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-8	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-9	2025-01-30	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-1	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-2	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-4	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-5	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-6	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-7	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-8	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-9	2020-03-06	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-1	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-2	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-4	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-5	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-6	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-7	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-8	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel
61577-3235-9	2020-01-31	Sore No More Cool Therapy Natural Pain Relieving Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61577-3235-1	SORE NO MORE COOL THERAPY	226.8 g in 1 JAR	GEL	226.8	12
61577-3235-2	SORE NO MORE COOL THERAPY	907.2 g in 1 BOTTLE, PUMP	GEL	907.2	12
61577-3235-4	SORE NO MORE COOL THERAPY	113.4 g in 1 JAR	GEL	113.4	12
61577-3235-5	SORE NO MORE COOL THERAPY	85 g in 1 BOTTLE, PLASTIC	GEL	85	12
61577-3235-6	SORE NO MORE COOL THERAPY	113.4 g in 1 TUBE	GEL	113.4	12
61577-3235-7	SORE NO MORE COOL THERAPY	56.7 g in 1 JAR	GEL	56.7	12
61577-3235-8	SORE NO MORE COOL THERAPY	28.3 g in 1 JAR	GEL	28.3	12
61577-3235-9	SORE NO MORE COOL THERAPY	5 g in 1 POUCH	GEL	5	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61577-3235	SORE NO MORE COOL THERAPY (MENTHOL) GEL [SOMBRA COSMETICS INC.]	12	Current NDC, Legacy NDC, 8 package rows	20250529_9aa1f0ac-3baf-4e45-9e3a-c28a99b22909.zip
61577-3235	ELEMAR PATCH (LIDOCAINE) KIT [V2 PHARMA, LLC]	11	Current NDC, Legacy NDC	20250101_3de6bb95-3673-45c4-bf11-90ec858c37d9.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 36 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
COLD AND HOT MEDICATED Patch	COLD AND HOT MEDICATED PATCH	Henan Enokon Medical Instrument Co., Ltd.	49aca763-be2a-cf38-e063-6294a90a092e	2026-01-31	Warnings	Exact identifier application number: M017
PAIN RELIEF HOT Patch	PAIN RELIEF HOT PATCH	Henan Enokon Medical Instrument Co., Ltd.	49ad128a-0f4c-085a-e063-6294a90ac9bb	2026-01-31	Warnings	Exact identifier application number: M017
Walgreens Chest Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Walgreen Company	3557d2e9-714a-4066-aa73-ea9e3363e574	2026-01-30	Warnings	Exact identifier application number: M017
Alveora HEMORRHOID MASTER	LIDOCAINE 4% PHENYLEPHRINE HCL 0.25% HEMORRHOID MASTER	Jiangxi Yudexi Pharmaceutical Co., LTD	4996f96a-898e-de01-e063-6394a90a3907	2026-01-30	Warnings	Exact identifier application number: M017
Sunburn Relief	LIDOCAINE HCL 0.5%	Rite Aid Corporation	b67af0c7-1ae8-4494-bb0e-d7f66ebca352	2026-01-30	Warnings, Adverse reactions	Exact identifier application number: M017
Drs Pharmacy PAIN RELIEF MUSCLE ARITHRITIS	CAPSAICIN	OL PHARMA TECH,LLC	48fdf9dc-05df-866d-e063-6294a90ae03a	2026-01-30	Warnings	Exact identifier application number: M017
ROCKTAPE GO Kinesiology Tape and Analgesic	MENTHOL, METHYL SALICYLATE	Implus Footcare, LLC	b779c7d8-dbe6-472f-9282-6cced25cfd2e	2026-01-29	Warnings	Exact identifier application number: M017
RockSauce Warming Massage	MENTHOL, METHYL SALICYLATE	Implus Footcare, LLC	de5f7add-1f2b-438a-ac17-753ebb53e697	2026-01-29	Warnings	Exact identifier application number: M017
RockSauce Warming Massage Roll-On	MENTHOL, METHYL SALICYLATE	Implus Footcare, LLC	5a2d9c3a-67fc-4c1a-b1e8-62a93880397a	2026-01-29	Warnings	Exact identifier application number: M017
Analgesic Dr. Collado	MENTHOL, METHYL SALICYLATE	Laboratorios Dr. Collado, S.A	c0dad2db-7c96-49b8-a451-bf8cfa7f798b	2026-01-29	Warnings	Exact identifier application number: M017
RockSauce Warming Massage	MENTHOL, METHYL SALICYLATE	Implus Footcare, LLC	3121c7f7-d7e5-4ca9-9057-03edf9c94c56	2026-01-29	Warnings	Exact identifier application number: M017
Analgesic Gel Dr. Collado Menthol 4 Methyl Salicylate	MENTHOL, METHYL SALICYLATE	Laboratorios Dr. Collado, S.A.	87c22e6f-3ab0-47c3-94ea-48b3d1a95d9d	2026-01-29	Warnings	Exact identifier application number: M017
ProCure Hydrocortisone Cream Plus	HYDROCORTISONE	Rooftop Consumer Health, Inc.	fe334cae-e019-4397-8498-df3c923ae8b5	2026-01-29	Warnings	Exact identifier application number: M017
Red Oil Pain Relief	CAMPHOR (SYNTHETIC), MENTHOL, PHENOL	The Red Oil Company Inc	1e36579a-72da-46ba-ac72-5960a11c0880	2026-01-29	Warnings	Exact identifier application number: M017
Extra Strength Balm	CAPSICUM, MENTHOL	NATURES FORMULAE HEALTH PRODUCTS LTD.	498a5e2a-4de0-561c-e063-6394a90ac05c	2026-01-29	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET POTENT PAIN RELIEF	45c76956-db3f-3e84-e063-6394a90adce1	2026-01-29	Warnings	Exact identifier application number: M017
PAIN RELIEF PATCHES	LIDOCAINE	WALMART STORES INC	b82cfe42-f521-4784-8c60-98481524c5ec	2026-01-29	Warnings	Exact identifier application number: M017
Equate Pain Relief Patch Camphor/Menthol/Salicylate	CAMPHOR, MENTHOL, METHYL SALICYLATE	Walmart Stores Inc	b869848c-21e2-5ca2-e053-2995a90a86f2	2026-01-29	Warnings	Exact identifier application number: M017
HEATING PAIN RELIEF	METHYL SALICYLATE, MENTHOL	SUNSET NOVELTIES, INC	498cd2aa-ee59-67b5-e063-6294a90ac242	2026-01-29	Warnings	Exact identifier application number: M017
COOLING PAIN RELIEF	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	498d76d8-788b-4cc7-e063-6294a90a1696	2026-01-29	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
415976	menthol 6 % Topical Gel	PSN	9aa1f0ac-3baf-4e45-9e3a-c28a99b22909	12
415976	menthol 0.06 MG/MG Topical Gel	SCD	9aa1f0ac-3baf-4e45-9e3a-c28a99b22909	12
415976	menthol 6 % Topical Gel	SY	9aa1f0ac-3baf-4e45-9e3a-c28a99b22909	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61577-3235-1	61577323501	226.8 g in 1 JAR (61577-3235-1)	226.8 g	2016-06-14	0000-00-00	No	No	Current
61577-3235-2	61577323502	907.2 g in 1 BOTTLE, PUMP (61577-3235-2)	907.2 g	2016-06-14	0000-00-00	No	No	Current
61577-3235-4	61577323504	113.4 g in 1 JAR (61577-3235-4)	113.4 g	2016-06-14	0000-00-00	No	No	Current
61577-3235-5	61577323505	85 g in 1 BOTTLE, PLASTIC (61577-3235-5)	85 g	2016-06-14	0000-00-00	No	No	Current
61577-3235-6	61577323506	113.4 g in 1 TUBE (61577-3235-6)	113.4 g	2016-06-14	0000-00-00	No	No	Current
61577-3235-7	61577323507	56.7 g in 1 JAR (61577-3235-7)	56.7 g	2016-06-14	0000-00-00	No	No	Current
61577-3235-8	61577323508	28.3 g in 1 JAR (61577-3235-8)	28.3 g	2017-07-02	0000-00-00	Yes	No	Current
61577-3235-9	61577323509	5 g in 1 POUCH (61577-3235-9)	5 g	2016-06-14	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Sore No More Cool Therapy Natural Pain Relieving Gel	SOMBRA COSMETICS INC.	2025-05-12	HUMAN OTC DRUG LABEL	12