Pain Relief

Product NDC: 47682-321
11-digit product format: 476820321
Labeler code: 47682
Product ID: 47682-321_3e4ee639-9aef-38c5-e063-6394a90a9ad3
Type: HUMAN OTC DRUG
Nonproprietary name: Analgesic Menthol
Dosage form: SPRAY
Route: TOPICAL
Labeler: Unifirst First Aid Corporation
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-04-01
Substance: MENTHOL
Active strength: 70 mg/L
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: Pain Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	70 mg/L

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 SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
8162d22d-04c0-de07-e053-2991aa0a9975	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
47682-321-02	Pain Relief	0.059 L in 1 BOTTLE, SPRAY	SPRAY	0.059		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
47682-321	PAIN RELIEF (ANALGESIC MENTHOL) SPRAY [UNIFIRST FIRST AID CORPORATION]	6	Current NDC, Legacy NDC, 1 package rows	20240117_8162d22d-04c0-de07-e053-2991aa0a9975.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 13 of 23 · 441 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dr Butlers Advanced Hemorrhoid Relief	LIDOCAINE HCL 5%, PHENYLEPHRINE HCL 0.25%, WITCH HAZEL 50%	Beyond Health. PA	3aa0ee7a-3863-254d-e063-6394a90ad40e	2025-07-23	Warnings	Exact identifier application number: M015
Dr. Butler Hemorrhoid Treatment	PHENYLEPHRINE HYDROCHLORIDE 0.25%, WITCH HAZEL 50%	Beyond Health P.A.	d2d1c81c-6443-c4b7-e053-2995a90a14d7	2025-07-22	Warnings	Exact identifier application number: M015
GoodSense Hemorrhoidal Pain Relief	GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL	Perrigo Direct, Inc	2e5f699d-45e8-6451-e063-6394a90a8ad8	2025-07-20	Warnings	Exact identifier application number: M015
Good Sense Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	L. Perrigo Company	379f8738-a871-4b09-abd1-c86386dfee04	2025-07-15	Warnings	Exact identifier application number: M015
Maximum Strength Hemorrhoidal Pads	WITCH HAZEL	Walmart, Inc.	6dd8d3d9-5109-4869-917b-9521e9ba1ed0	2025-07-14	Warnings	Exact identifier application number: M015
Nikzon Hemorrhoidal	GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, AND PRAMOXINE HYDROCHLORIDE	Genomma Lab USA	8f9a9939-2c99-489f-b597-9a51ec2684f9	2025-07-14	Warnings	Exact identifier application number: M015
ReVIVOL-XR	PHENYLEPHRINE HYDROCHLORIDE	Unipack LLC	2950fe83-a2a4-4ed4-b645-69d6fd2381ae	2025-07-13	Warnings	Exact identifier application number: M015
medicated wipes	WITCH HAZEL	Meijer Distribution Inc.	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	2025-07-11	Warnings	Exact identifier application number: M015
hemorrhoidal pads	WITCH HAZEL	Meijer Distribution Inc.	53e39d22-a89e-4f95-8c64-abeb50f72ce7	2025-07-11	Warnings	Exact identifier application number: M015
INVIGOR OH	LIDOCAINE	Natureplex LLC	7c7b536d-e41a-4017-9df9-982e2e9cfe4e	2025-07-10	Warnings	Exact identifier application number: M015
Maximum Strength Hemorrhoidal Cream with Aloe	GLYCERIN, PHENYLEPHINE HCI, PRAMOXINE HCI, PETROLATUM	Chain Drug Marketing Association	396ea654-8be1-591a-e063-6294a90a11e2	2025-07-08	Warnings	Exact identifier application number: M015
PREPARATION H SOOTHING RELIEF ANTI-ITCH	HYDROCORTISONE	Haleon US Holdings LLC	d6148d77-ef6f-4552-b5ba-43b429923f19	2025-07-07	Warnings	Exact identifier application number: M015
Rectal Care Cream	RECTAL CARE CREAM	Allegiant Health	ce585082-ad39-4b6f-a756-0d9a81a13eb8	2025-07-07	Warnings	Exact identifier application number: M015
Bisacodyl Laxative	BISACODYL LAXATIVE SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35cb0386-a662-6893-e063-6294a90aa71a	2025-07-03	Warnings	Exact identifier application number: M015
Hemorrhoidal Cream	GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM	Trifecta Pharmaceuticals Usa Llc	38cf4e43-280b-eb96-e063-6294a90a5949	2025-07-02	Warnings	Exact identifier application number: M015
TN Dickinsons Medicated Cooling Foam Hemorrhoidal Relief	WITCH HAZEL	Dickinson Brands Inc.	deca8ae2-53a3-4c90-aa10-45354e2cdab8	2025-06-27	Warnings	Exact identifier application number: M015
Glycerin Laxative	GLYCERIN LAXATIVE SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35cc266a-196f-16ce-e063-6394a90a24af	2025-06-20	Warnings	Exact identifier application number: M015
Phenylephrine Hemorrhoidal	HEMORRHOIDAL SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35ccb320-e902-3d1a-e063-6294a90a68d5	2025-06-20	Warnings	Exact identifier application number: M015
ProCure Hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Twin Med LLC	37a4cc43-0d53-f1bf-e063-6394a90a2dc9	2025-06-15	Warnings	Exact identifier application number: M015
Hemorrhoidal Pain Relief	HEMORRHOIDAL PAIN RELIEF OINTMENT	Neilmed Pharmaceuticals Inc.	374d89b6-9305-9adf-e063-6394a90adb32	2025-06-11	Warnings	Exact identifier application number: M015

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
47682-321-02	47682032102	.059 L in 1 BOTTLE, SPRAY (47682-321-02)	2019-04-01	0000-00-00	No	No	Current