Salonpas DEEP Relieving

Product NDC: 55328-900
11-digit product format: 553280900
Labeler code: 55328
Product ID: 55328-900_91461b7c-ddbc-442a-940e-67f9053580f5
Type: HUMAN OTC DRUG
Nonproprietary name: Camphor, Menthol, Methyl salicylate
Dosage form: GEL
Route: PERCUTANEOUS; TOPICAL; TRANSDERMAL
Labeler: Hisamitsu America, Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2013-06-01
Substance: CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Active strength: 3.1; 10; 15 g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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: Salonpas DEEP Relieving
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	3.1 g/100g
MENTHOL	10 g/100g
METHYL SALICYLATE	15 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup
LAV5U5022Y	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1425325	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
a4ddb2b9-d023-4c8c-9285-93d51f93207d	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55328-900-02	Salonpas DEEP Relieving	78 g in 1 TUBE	GEL	78		4
55328-900-02	Salonpas DEEP Relieving	1 in 1 BOX	GEL	1		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
55328-900-02	GM - Gram	55328-900	78b637e9-1b18-4c58-b243-9563c7ab45b6	1	2024-04-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
METHYL SALICYLATE	ACTIVE INGREDIENT	LAV5U5022Y	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER	INACTIVE INGREDIENT	W59H9296ZG	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
DIMETHYL ISOSORBIDE	INACTIVE INGREDIENT	SA6A6V432S	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55328-900	SALONPAS DEEP RELIEVING (CAMPHOR, MENTHOL, METHYL SALICYLATE) GEL [HISAMITSU AMERICA, INC.]	4	Current NDC, Legacy NDC, 2 package rows	20241205_a4ddb2b9-d023-4c8c-9285-93d51f93207d.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 65 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hempvana Cold As Ice Pain Relief	MENTHOL	Telebrands Corp	95e84bb9-ba2e-5009-e053-2995a90a4362	2025-11-12	Warnings	Exact identifier application number: M017
Lidozall	LIDOCAINE HYDROCHLORIDE	V2 Pharma LLC	1eb2dfb2-3ad1-488b-aed9-17220e34a10c	2025-11-12	Warnings	Exact identifier application number: M017
Lidozall Plus	LIDOCAINE HYDROCHLORIDE	V2 Pharma LLC	ba3cbb15-f4ed-443e-af43-a758481acb0b	2025-11-12	Warnings	Exact identifier application number: M017
Knee Pain Relief Patch	DL-CAMPHOR, L-MENTHOL, METHYL SALICYLATE	Shenzhen Finona Information Technology Co., Ltd	38755738-1a06-fdb4-e063-6294a90aa6eb	2025-11-12	Warnings	Exact identifier application number: M017
Recovery Numb	LIDOCAINE 4%	PURKLENZ FORMULATIONS INC.	e95e38e3-f743-4f5c-abdf-99ba6856e6f7	2025-11-12	Warnings	Exact identifier application number: M017
Rapid Relief	COLD RELIEF PATCH 5% MENTHOL	RAPID AID VIET NAM COMPANY LIMITED	434c13c2-52ee-000f-e063-6294a90af7e7	2025-11-11	Warnings	Exact identifier application number: M017
Rapid Relief	PAIN RELIEF PATCH CAMPHOR 110MG MENTHOL 33MG CAPSICUM EXTRACT 22MG	RAPID AID VIET NAM COMPANY LIMITED	434d5f92-05c2-d884-e063-6394a90ad28c	2025-11-11	Warnings	Exact identifier application number: M017
Rapid Relief	PAIN RELIEF PATCH LIDOCAINE 4% MENTHOL 1%	RAPID AID VIET NAM COMPANY LIMITED	434df0be-49ff-aa56-e063-6394a90a3b5a	2025-11-11	Warnings	Exact identifier application number: M017
TopCare Pain Relief Maximum Strength	LIDOCAINE HYDROCHLORIDE	TOPCO ASSOCIATES	b0ae3a7c-52d1-4923-bd50-6bb3749006c8	2025-11-11	Warnings	Exact identifier application number: M017
Comfortcaine	LIDOCAINE HCL	QS Key West Aloe, LLC	831b7c11-e437-4e74-808e-c9c1eb8b82f6	2025-11-11	Warnings	Exact identifier application number: M017
A and E Marathon Delay Serum	DELAY SERUM	Phe Inc	4355d1d8-44fe-aca1-e063-6294a90a85ff	2025-11-11	Warnings	Exact identifier application number: M017
A and E Deep Throat Desensitizing SprayStrawberry	ORAL NUMBING SPRAY STRAWBERRY	Phe Inc	4355dab1-a293-ded6-e063-6394a90af9b0	2025-11-11	Warnings	Exact identifier application number: M017
A and E Easy Anal Gel	ANAL NUMBING LUBRICANT	Phe Inc	4355e0f3-65ba-eca6-e063-6394a90ab43c	2025-11-11	Warnings	Exact identifier application number: M017
A and E Deep Throat Desensitizing SprayPeppermint	ORAL NUMBING SPRAY MINT	Phe Inc	4355e0d0-1222-d594-e063-6294a90abb29	2025-11-11	Warnings	Exact identifier application number: M017
DermaNumb Analgesic	LIDOCAINE HCL	A.T.S. Laboratories, LLC	0ea46890-45c3-4732-bc47-227f7c67daf1	2025-11-11	Warnings	Exact identifier application number: M017
Derma Numb Pain Relief	LIDOCAINE HCL	A.T.S. Laboratories, LLC	710991ae-8f82-4893-93a7-0ef3f815d132	2025-11-11	Warnings	Exact identifier application number: M017
HYDROCORTISONE	HYDROCORTISONE	Encube Ethicals, Inc.	969cd576-82d3-4662-bbc1-3587a1f6a564	2025-11-10	Warnings	Exact identifier application number: M017
Jelcaine Sterile	LIDOCAINE HCL JELLY USP, 2%	Brookfield Pharmaceuticals, LLC	1a39d1de-7aa2-3068-e063-6394a90aed85	2025-11-10	Warnings	Exact identifier application number: M017
Hush Anesthetic	LIDOCAINE	HUSH Anesthetic	c6e86a0f-6f9b-45b7-86ce-0bb1c198061a	2025-11-10	Warnings	Exact identifier application number: M017
Hush Anesthetic	LIDOCAINE	HUSH Anesthetic	97ae1993-7268-4b7f-92e2-6004337d5650	2025-11-10	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)
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1425325	camphor 3.1 % / menthol 10 % / methyl salicylate 15 % Topical Gel	PSN	a4ddb2b9-d023-4c8c-9285-93d51f93207d	4
1425325	camphor 0.031 MG/MG / menthol 0.1 MG/MG / methyl salicylate 0.15 MG/MG Topical Gel	SCD	a4ddb2b9-d023-4c8c-9285-93d51f93207d	4
1425325	camphor 3.1 % / menthol 10 % / methyl salicylate 15 % Topical Gel	SY	a4ddb2b9-d023-4c8c-9285-93d51f93207d	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55328-900-02	55328090002	1 TUBE in 1 BOX (55328-900-02) / 78 g in 1 TUBE	1 tube	2013-06-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Salonpas DEEP Relieving - Hisamitsu America, Inc.	Hisamitsu America, Inc.	2024-12-03	HUMAN OTC DRUG LABEL	4