CVS Pain Relief Lavender Scent

Product NDC: 51316-118
11-digit product format: 513160118
Labeler code: 51316
Product ID: 51316-118_484b0833-9f89-f155-e063-6294a90a1869
Type: HUMAN OTC DRUG
Nonproprietary name: Menthol 4%
Dosage form: GEL
Route: TOPICAL
Labeler: CVS
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2026-06-01
Substance: MENTHOL, (+)-
Active strength: 4 g/100mL
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: CVS Pain Relief Lavender Scent
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, (+)-	4 g/100mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
C6B1OE8P3W	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
415974	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
484b0833-9f8a-f155-e063-6294a90a1869	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

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 107 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DCH Labs Cool and Heat Roll-On	MENTHOL 16%	Derma Care Research Labs, LLC	d35d7720-44ce-3624-e053-2995a90a7fb4	2024-12-19	Warnings	Exact identifier application number: M017
Dr Goldsons Pain	MENTHOL 8%, METHYL SALICYLATE 30%	Derma Care Research Labs, LLC	fb34b0d3-ccc0-305e-e053-6394a90a231d	2024-12-19	Warnings	Exact identifier application number: M017
Warrior Pain Relieving	CAMPHOR 4%, MENTHOL 10%, METHYL SALICYLATE 30%	Derma Care Research Labs, LLC	dd06af3c-5452-9759-e053-2a95a90afc21	2024-12-19	Warnings	Exact identifier application number: M017
Warrior Burn Relief Aloe Maximum Strength	LIDOCAINE HCL 4%	Derma Care Research Labs, LLC	ec6efa4b-dcbe-1c2b-e053-2995a90ae043	2024-12-19	Warnings	Exact identifier application number: M017
DCH Arthritis Relief	TROLAMIN SALICYLATE 10%	Derma Care Research Labs, LLC	ff31e515-5780-b77d-e053-6394a90af6b9	2024-12-19	Warnings	Exact identifier application number: M017
DCH Pain Relief	LIDOCAINE 4%	Derma Care Research Labs, LLC	00efda74-d434-04be-e063-6294a90a6d98	2024-12-19	Warnings	Exact identifier application number: M017
Dollar General Cold Therapy Pain Relief	MENTHOL 5%	Dolgencorp, LLC	ff3284d1-e73c-93bf-e053-6294a90aaf4e	2024-12-19	Warnings	Exact identifier application number: M017
Dollar General Pain Relieving Patch with Lidocaine	LIDOCAINE	DOLGENCORP, LLC	55828cd1-3a1e-48ac-bb01-4c50b96d09a2	2024-12-19	Warnings	Exact identifier application number: M017
DCH Nerve Pain Relief	LIDOCAINE 4%, MENTHOL 1%	Derma Care Research Labs, LLC	00db480a-e510-a64d-e063-6394a90a4695	2024-12-19	Warnings	Exact identifier application number: M017
Pain, Burn, and Itch Relief	BENZOCAINE 20%, MENTHOL 0.5%	Derma Care Research Labs, LLC	fd9fe09f-3ae9-c5f5-e053-6394a90ad691	2024-12-19	Warnings	Exact identifier application number: M017
DCH Cooling Pain Relief	MENTHOL 4%	Derma Care Research Labs, LLC	00ed3175-c3ba-6545-e063-6394a90acfd1	2024-12-19	Warnings	Exact identifier application number: M017
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

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
C6B1OE8P3W	MENTHOL, (+)-	15356-60-2	MENTHOL, (+)-

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
51316-118-02	51316011802	74 mL in 1 BOTTLE, PLASTIC (51316-118-02)	74 ml	2026-06-01	No	No	Current
51316-118-03	51316011803	89 mL in 1 TUBE (51316-118-03)	89 ml	2026-06-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
CVS Pain Relief Lavender Scent, Menthol 4%	CVS \| Derma Care Research Labs, LLC	2026-01-13	HUMAN OTC DRUG LABEL	1