SORE NO MORE

Product NDC: 61577-2280
11-digit product format: 615772280
Labeler code: 61577
Product ID: 61577-2280_4d785eb6-f915-92cc-e063-6294a90ad2f4
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL CAMPHOR
Dosage form: GEL
Route: TOPICAL
Labeler: SOMBRA COSMETICS INC.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2016-10-25
Substance: MENTHOL; CAMPHOR (SYNTHETIC)
Active strength: .03; .03 g/g; g/g
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 35 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	61577-2280-4	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-2280-2	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-2280-5	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	61577-2280-8	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	61577-2280-4	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-2280-2	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-2280-5	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	61577-2280-8	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	61577-2280-4	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-2280-2	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-2280-5	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	61577-2280-8	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	61577-2280-4	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-2280-2	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-2280-5	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	61577-2280-8	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	61577-2280-2	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-2280-5	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-2280-4	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	61577-2280-8	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	61577-2280-2	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-2280-5	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-2280-4	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	61577-2280-8	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	61577-2280-2	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-2280-5	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-2280-4	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	61577-2280-8	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
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	.03 g/g
CAMPHOR (SYNTHETIC)	.03 g/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
L7T10EIP3A	Internal UNII lookup
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
630714	Internal RxNorm lookup
1372559	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
80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
61577-2280-2	2025-01-30	Glo Germ SORE NO MORE
61577-2280-4	2025-01-30	Glo Germ SORE NO MORE
61577-2280-5	2025-01-30	Glo Germ SORE NO MORE
61577-2280-8	2025-01-30	Glo Germ SORE NO MORE
61577-2280-2	2023-03-08	Glo Germ SORE NO MORE
61577-2280-4	2023-03-08	Glo Germ SORE NO MORE
61577-2280-5	2023-03-08	Glo Germ SORE NO MORE
61577-2280-8	2023-03-08	Glo Germ SORE NO MORE
61577-2280-2	2023-01-30	Glo Germ SORE NO MORE
61577-2280-4	2023-01-30	Glo Germ SORE NO MORE
61577-2280-5	2023-01-30	Glo Germ SORE NO MORE
61577-2280-8	2023-01-30	Glo Germ SORE NO MORE
61577-2280-2	2020-03-06	Glo Germ SORE NO MORE
61577-2280-4	2020-03-06	Glo Germ SORE NO MORE
61577-2280-5	2020-03-06	Glo Germ SORE NO MORE
61577-2280-8	2020-03-06	Glo Germ SORE NO MORE
61577-2280-2	2020-01-31	Glo Germ SORE NO MORE
61577-2280-4	2020-01-31	Glo Germ SORE NO MORE
61577-2280-5	2020-01-31	Glo Germ SORE NO MORE
61577-2280-8	2020-01-31	Glo Germ SORE NO MORE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61577-2280-2	SORE NO MORE	58.7 g in 1 JAR	GEL	58.7	7
61577-2280-4	SORE NO MORE	113.4 g in 1 JAR	GEL	113.4	7
61577-2280-5	SORE NO MORE	5 g in 1 POUCH	GEL	5	7
61577-2280-6	SORE NO MORE	18200 g in 1 PAIL	GEL	18200	7
61577-2280-8	SORE NO MORE	226.8 g in 1 JAR	GEL	226.8	7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
ALOE VERA LEAF	INACTIVE INGREDIENT	ZY81Z83H0X	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
CAPSICUM	INACTIVE INGREDIENT	00UK7646FG	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
CARBOMER HOMOPOLYMER TYPE C	INACTIVE INGREDIENT	4Q93RCW27E	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
DECYL GLUCOSIDE	INACTIVE INGREDIENT	Z17H97EA6Y	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
FILIPENDULA ULMARIA FLOWER	INACTIVE INGREDIENT	06L18L32G6	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
GRAPEFRUIT SEED OIL	INACTIVE INGREDIENT	598D944HOL	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
GREEN TEA LEAF	INACTIVE INGREDIENT	W2ZU1RY8B0	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
ORANGE PEEL	INACTIVE INGREDIENT	TI9T76XD44	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
ROSA CENTIFOLIA FLOWER OIL	INACTIVE INGREDIENT	H32V31VMWY	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
SODIUM HYDROXYMETHYLGLYCINATE	INACTIVE INGREDIENT	DIG6BWZ9XT	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
WITCH HAZEL	INACTIVE INGREDIENT	101I4J0U34	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1
YUCCA SCHIDIGERA ROOT	INACTIVE INGREDIENT	E2H9ET15AT	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61577-2280	SORE NO MORE (MENTHOL CAMPHOR) GEL [SOMBRA COSMETICS INC.]	5	Current NDC, Legacy NDC, 5 package rows	20230309_80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd.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 92 of 151 · 3,010 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SORE NO MORE COOL THERAPY	MENTHOL	SOMBRA COSMETICS INC.	9aa1f0ac-3baf-4e45-9e3a-c28a99b22909	2025-05-12	Warnings	Exact identifier application number: M017
Calm and Correct Serum with Lidocaine	LIDOCAINE 3 PERCENT	Renu Laboratories, LLC	ddcf1c2e-2f67-44d7-e053-2a95a90a812b	2025-05-09	Warnings	Exact identifier application number: M017
Mqupin Knee Patch	KNEE PATCH	Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd	09772e4b-8193-3771-e063-6394a90a9516	2025-05-08	Warnings	Exact identifier application number: M017
Hydrocortisone Cream	HYDROCORTISONE	Trifecta Pharmaceuticals USA	d57a59fb-c8f2-f73b-e053-2995a90a4cdb	2025-05-08	Warnings	Exact identifier application number: M017
Hydrocortisone Cream	HYDROCORTISONE	Trifecta Pharmaceuticals USA	4c96ec41-841c-322b-e054-00144ff8d46c	2025-05-08	Warnings	Exact identifier application number: M017
GNP Extra Strength Anti-Itch Cream	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	Amerisource Bergen	34a66224-ef3c-e36e-e063-6394a90ac99d	2025-05-08	Warnings	Exact identifier application number: M017
Good Neighbor Muscle Rub Cream	CAMPHOR 4.0%, MENTHOL 10.0%, METHYL SALICYLATE 30.0%,	Amerisource Bergen	34924bb9-e3e8-70e6-e063-6294a90aaa8c	2025-05-07	Warnings	Exact identifier application number: M017
DermaRad Relief Post Radiation Calming	LIDOCAINE 3 PERCENT	Renu Laboratories, LLC	e5d64929-fb9c-7ebc-e053-2995a90a9318	2025-05-07	Warnings	Exact identifier application number: M017
Cold Hot Medicated Patch 5% Menthol	MENTHOL	InterMed Laboratories Private Limited	33ee0235-5a6e-0ea1-e063-6394a90a89a5	2025-05-06	Warnings	Exact identifier application number: M017
DermaRad Relief	LIDOCAINE EMULSION	RENU LABORATORIES, LLC	d5e11f73-918b-eeac-e053-2995a90a4a83	2025-05-06	Warnings	Exact identifier application number: M017
Plantar Fasciitis Pain Relief Gel-Patch	LIDOCAINE, MENTHOL	Guangzhou Zhupuyou E-commerce Co., Ltd	34838622-b092-afeb-e063-6294a90ae7db	2025-05-06	Warnings	Exact identifier application number: M017
Climax Shield Delay	BENZOCAINE	PRODUCT MAX GROUP INC	9c720cdc-f753-47ce-95ff-3b26e461a0ab	2025-05-05	Warnings	Exact identifier application number: M017
PediFix Lidocaine Pain-Relief Patches	LIDOCAINE PAIN-RELIEF PATCHES	PediFix, Inc	346550b9-d2ba-184e-e063-6394a90a591a	2025-05-05	Warnings	Exact identifier application number: M017
Walgreens Stop Itch Gel	DIPHENHYDRAMINE HCL	Walgreens Co	23586336-8f46-3dcd-e063-6394a90accc9	2025-05-04	Warnings	Exact identifier application number: M017
WaxRx EarAcheRx Pain Relieving Drops	4% LIDOCAINE HCL	DOCTOR EASY MEDICAL PRODUCTS, LLC	34156655-8706-f0a4-e063-6294a90acc90	2025-05-01	Warnings	Exact identifier application number: M017
foster and thrive anti itch cream	DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE	Strategic Sourcing Services LLC	bb08293d-5db8-4cc8-9fe3-bd02061dbeb9	2025-04-30	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch	LIDOCAINE	Solis Pharmaceuticals Inc.	3061d301-2104-b1b2-e063-6394a90a9b6e	2025-04-29	Warnings	Exact identifier application number: M017
Maximum Strength 4% Lidocaine Patch	LIDOCAINE	InterMed Laboratories Private Limited	33ed754e-8852-d5b2-e063-6394a90a7cf2	2025-04-29	Warnings	Exact identifier application number: M017
Cold Hot Medicated Patch 5% Menthol	MENTHOL	InterMed Laboratories Private Limited	33ee6e48-243e-4ded-e063-6394a90a987d	2025-04-29	Warnings	Exact identifier application number: M017
Lidocaine Pain Relief Gel-Patch	LIDOCAINE	Guangzhou Zhupuyou E-commerce Co., Ltd	32b96689-8e9b-4c2e-e063-6294a90a7d1c	2025-04-29	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
630714	camphor 3 % / menthol 3 % Topical Gel	PSN	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	7
1372559	Sore No More 3 % / 3 % Topical Gel	PSN	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	7
1372559	camphor 0.03 MG/MG / menthol 0.03 MG/MG Topical Gel [Sore No More]	SBD	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	7
630714	camphor 0.03 MG/MG / menthol 0.03 MG/MG Topical Gel	SCD	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	7
630714	camphor 3 % / menthol 3 % Topical Gel	SY	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	7
1372559	Sore No More (camphor 3 % / menthol 3 % ) Topical Gel	SY	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61577-2280-2	61577228002	58.7 g in 1 JAR (61577-2280-2)	58.7 g	2016-10-25	0000-00-00	No	No	Current
61577-2280-4	61577228004	113.4 g in 1 JAR (61577-2280-4)	113.4 g	2016-10-25	0000-00-00	No	No	Current
61577-2280-5	61577228005	5 g in 1 POUCH (61577-2280-5)	5 g	2016-10-25	0000-00-00	No	No	Current
61577-2280-6	61577228006	18200 g in 1 PAIL (61577-2280-6)	18200 g	2026-03-20		No	No	Current
61577-2280-8	61577228008	226.8 g in 1 JAR (61577-2280-8)	226.8 g	2016-10-25	0000-00-00	No	No	Current