Valtrum Topical Analgesic Roll On

Product NDC: 75849-301
11-digit product format: 758490301
Labeler code: 75849
Product ID: 75849-301_e0089b62-e19a-4ab7-a2f0-a8e9a70ff2e8
Type: HUMAN OTC DRUG
Nonproprietary name: SALICYLIC ACID MENTHOL CAMPHOR (NATURAL)
Dosage form: GEL
Route: TOPICAL
Labeler: LABORATORIOS QUANTIUM LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-03-01
Substance: METHYL SALICYLATE; MENTHOL, UNSPECIFIED FORM; CAMPHOR (NATURAL)
Active strength: 10; 3; 3 g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2026-12-31
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: Valtrum Topical Analgesic Roll On
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
METHYL SALICYLATE	10 g/100g
MENTHOL, UNSPECIFIED FORM	3 g/100g
CAMPHOR (NATURAL)	3 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
LAV5U5022Y	Internal UNII lookup
L7T10EIP3A	Internal UNII lookup
N20HL7Q941	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2123377	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
28167e2a-9afb-44e7-90c7-9577df9504b6	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
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2023-11-28	28167e2a-9afb-44e7-90c7-9577df9504b6
2023-01-30	28167e2a-9afb-44e7-90c7-9577df9504b6
2021-08-25	28167e2a-9afb-44e7-90c7-9577df9504b6
2021-01-29	28167e2a-9afb-44e7-90c7-9577df9504b6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75849-301-03	Valtrum Topical Analgesic Roll On	90 g in 1 TUBE, WITH APPLICATOR	GEL	90		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75849-301	VALTRUM TOPICAL ANALGESIC ROLL ON (SALICYLIC ACID MENTHOL CAMPHOR (NATURAL)) GEL [LABORATORIOS QUANTIUM LLC]	3	Current NDC, Legacy NDC, 1 package rows	20231129_28167e2a-9afb-44e7-90c7-9577df9504b6.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 67 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Overtime	METHYL SALICYLATE, MENTHOL AND CAPSAICIN	Physicians Science & Nature Inc.	25fec070-8587-42d1-ba6f-1a9c150acc98	2025-11-10	Warnings	Exact identifier application number: M017
Dendracin Neurodendraxcin	METHYL SALICYLATE, MENTHOL AND CAPSAICIN	Physicians Science & Nature Inc.	05742cd5-ece2-4007-bdf0-46b76d23df74	2025-11-10	Warnings	Exact identifier application number: M017
Anal Blu	DESENSITIZER	Novelties by Nasswalk, Inc.	03b9555b-c3ff-4baa-e063-6394a90afb2c	2025-11-10	Warnings	Exact identifier application number: M017
Stallion	DELAY CREME	Novelties by Nasswalk, Inc.	0261ec88-8fe4-d5f8-e063-6294a90ab3d4	2025-11-10	Warnings	Exact identifier application number: M017
ANAL-ESE	DESENSITIZER	Novelties by Nasswalk, Inc.	03b89eed-b433-a263-e063-6294a90a675b	2025-11-10	Warnings	Exact identifier application number: M017
Instant Erection	ULTIMATE ERECTION ENHANCER	Novelties by Nasswalk, Inc.	03a444f9-7052-0c38-e063-6294a90a4e56	2025-11-10	Warnings	Exact identifier application number: M017
STA-HARD	DESENSITIZING LUBRICANT	Novelties by Nasswalk, Inc.	02ef794b-8e70-5c26-e063-6294a90a28d1	2025-11-10	Warnings	Exact identifier application number: M017
ANAL-ESE	DESENSITIZER	Novelties by Nasswalk, Inc.	03a4a7ce-4cff-a608-e063-6294a90ad65d	2025-11-10	Warnings	Exact identifier application number: M017
FOOTSPA PEDI	ALCOHOL	CHEMCO CORPORATION	04de4392-74f6-7df8-e063-6294a90ae3b1	2025-11-08	Warnings	Exact identifier application number: M017
Johnson and Johnson All Purpose First Aid Kit	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	5cdb47c5-7951-4279-8a05-0a3199d3dd45	2025-11-06	Warnings	Exact identifier application number: M017
Johnson and Johnson First Aid Travel Ready 80 CT	ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	f388f105-48ba-4616-e053-2a95a90a0049	2025-11-06	Warnings	Exact identifier application number: M017
Johnson and Johnson First Aid All Purpose 160 CT	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	Kenvue Brands LLC	f3933330-2550-4a88-e053-2a95a90a3997	2025-11-06	Warnings	Exact identifier application number: M017
Foot and Leg Pain Relief	LIDOCAINE	Premier Brands of America Inc.	42f23e2f-11c6-da49-e063-6294a90ac720	2025-11-06	Warnings	Exact identifier application number: M017
HEALING TREE CALMING ANTI-ITCH	HYDROCORTISONE	Renu Laboratories, LLC	fc8bcde9-26e8-a35f-e053-6394a90a3300	2025-11-06	Warnings	Exact identifier application number: M017
Calamine Plus	CALAMINE PLUS PRAMOXINE HCL	Chain Drug Marketing Association Inc	1a3f8819-58cf-8923-e063-6394a90a37af	2025-11-06	Warnings	Exact identifier application number: M017
Extra Strength Itch Relief	DIPHENHYDRAMINE HCL AND ZINC ACETATE	Chain Drug Marketing Association Inc	1a2997bc-7741-e658-e063-6394a90af6fd	2025-11-06	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF CONTINUOUS SPRAY	Topco Associates LLC	8026c7dd-eb7b-ebea-e053-2991aa0a1b0f	2025-11-06	Warnings	Exact identifier application number: M017
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF	Walgreen Company	6057b4ff-6adc-4688-893c-62d237d7d1ae	2025-11-06	Warnings	Exact identifier application number: M017
BANPINGHUA Glucosamine Chondroitin Patch	PEPPERMINT, CAMPHOR, BORNEOL	Henan Lijitang Medical Technology Co., Ltd.	42f8c2ae-50a2-2358-e063-6394a90a5979	2025-11-06	Warnings	Exact identifier application number: M017
PAINGEL	CAMPHOR, MENTHOL	NACOR BUSINESS GROUP LLC	42fa2397-b61a-3b16-e063-6294a90a5fed	2025-11-06	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
LAV5U5022Y	METHYL SALICYLATE	119-36-8	METHYL SALICYLATE
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM
N20HL7Q941	CAMPHOR (NATURAL)	464-49-3	CAMPHOR (NATURAL)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2123377	camphor 3 % / menthol 3 % / methyl salicylate 10 % Topical Gel	PSN	28167e2a-9afb-44e7-90c7-9577df9504b6	3
2123377	camphor 0.03 MG/MG / menthol 0.03 MG/MG / methyl salicylate 0.1 MG/MG Topical Gel	SCD	28167e2a-9afb-44e7-90c7-9577df9504b6	3
2123377	camphor 3 % / menthol 3 % / methyl salicylate 10 % Topical Gel	SY	28167e2a-9afb-44e7-90c7-9577df9504b6	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
75849-301-03	75849030103	90 g in 1 TUBE, WITH APPLICATOR (75849-301-03)	90 g	2019-03-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
METHYL SALICYLATE - LABORATORIOS QUANTIUM LLC \| GADAL Laboratories, Inc	LABORATORIOS QUANTIUM LLC \| GADAL Laboratories, Inc	2023-11-09	HUMAN OTC DRUG LABEL	3