ORCA Pain Reliever Putty with Menthol

Product NDC: 82939-001
11-digit product format: 829390001
Labeler code: 82939
Product ID: 82939-001_09ce4763-a8e6-7cff-e063-6294a90a851c
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: PASTE
Route: ORAL
Labeler: ORCA Products, LLC
Application: M022
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-09-15
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 8.4 mg/.525g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	82939-001	82939-001-01	D	Discontinued by firm		2026-10-21

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 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`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: ORCA Pain Reliever Putty with Menthol
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	8.4 mg/.525g

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
188cb01a-3d0f-43d9-983e-6475c0c5b06e	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
82939-001-01	ORCA Pain Reliever Putty with Menthol	1 in 1 PACKAGE	PASTE	1	3
82939-001-01	ORCA Pain Reliever Putty with Menthol	4.2 g in 1 JAR	PASTE	4.2	3
82939-001-02	ORCA Pain Reliever Putty with Menthol	1 in 1 BLISTER PACK	PASTE	1	3
82939-001-02	ORCA Pain Reliever Putty with Menthol	7 g in 1 JAR	PASTE	7	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82939-001	ORCA PAIN RELIEVER PUTTY WITH MENTHOL (MENTHOL) PASTE [ORCA PRODUCTS, LLC]	3	Current NDC, Legacy NDC, 4 package rows	20231111_188cb01a-3d0f-43d9-983e-6475c0c5b06e.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 18 of 40 · 782 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Giltuss Bucalsep	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Gil Pharmaceutical Corp	85053391-8d71-ab4f-e053-2991aa0a7e08	2025-10-09	Warnings	Exact identifier application number: M022
Listerine Gum Therapy Mouthwash Glacier Mint	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Kenvue Brands LLC	40a0bdf3-1698-1449-e063-6394a90ab13d	2025-10-08	Warnings	Exact identifier application number: M022
Kalaya Breath Refresh	MOUTHWASH	Avaria Health and Beauty Corp	750e99ff-72e4-3c2f-e053-2a91aa0ad5a0	2025-10-08	Warnings	Exact identifier application number: M022
Trader Joes	SODIUM FLUORIDE 0.24% AND POTASSIUM NITRATE 5%	TRADER JOE'S COMPANY	159abeba-6da2-2643-e063-6394a90a730d	2025-10-08	Warnings	Exact identifier application number: M022
Family Wellness Oral Pain Relief	BENZOCAINE 20%	FAMILY DOLLAR SERVICES INC	105d87d6-9147-43d4-e063-6394a90a57ee	2025-10-08	Warnings	Exact identifier application number: M022
Equate Glistening Mint	SODIUM FLUORIDE	Walmart Inc.	39ff21ee-a362-014e-e063-6294a90a0d91	2025-10-03	Warnings	Exact identifier application number: M022
Mouth Sore Relief Professional Strength	BENZOCAINE	CVS Pharmacy	1b7209f6-8368-47fa-8df2-b049613b8c1b	2025-09-30	Warnings	Exact identifier application number: M022
Hydrogen Peroxide	HYDROGEN PEROXIDE	Family Dollar (FAMILY WELLNESS)	9db73da2-5b70-41e6-bcf9-caa7f1142024	2025-09-29	Warnings	Exact identifier application number: M022
Esunix Oral Bacteriostatic Liquid	CETYLPYRIDINIUM CHLORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f47d7e1-b6ae-efd1-e063-6394a90a4602	2025-09-27	Warnings	Exact identifier application number: M022
Chloraseptic Sore Throat Cherry	PHENOL	Prestige Brands Holdings, Inc.	d5d62f7a-8f92-4d42-a2fb-691f896f72fc	2025-09-26	Warnings	Exact identifier application number: M022
Giltuss Bucalsep	BENZOCAINE, MENTHOL, ZINC CHLORIDE	Dextrum Laboratories Inc.	3fa233dc-156c-1e95-e063-6294a90a8bbd	2025-09-25	Warnings	Exact identifier application number: M022
Finafta MultiOral	BENZOCAINE	Dextrum Laboratories Inc.	cb027ab8-4175-4cc0-a73e-991dfb113df9	2025-09-23	Warnings	Exact identifier application number: M022
4-in-1 Teeth Care Pens	4-IN-1 TEETH CARE PENS	Jiangxi Dentalbright Technology Co., Ltd	3f872924-0c44-267b-e063-6394a90a1a67	2025-09-23	Warnings	Exact identifier application number: M022
Dental Relief	BENZOCAINE	Cintas Corporation	0f40f775-797e-43cf-88c9-00eea666494f	2025-09-23	Warnings	Exact identifier application number: M022
Seavue Anti-caries Gel	SODIUM FLUORIDE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f4c6086-b96d-8fa4-e063-6294a90ad800	2025-09-21	Warnings	Exact identifier application number: M022
Seavue Dental Desensitizer	POTASSIUM NITRATE AND SODIUM FLUORIDE DENTIFRICE	Xiling (Zhenjiang) Medical Technology Co., Ltd.	3f47f399-1a14-5264-e063-6394a90aeb1c	2025-09-20	Warnings	Exact identifier application number: M022
Povi-One	POVIDONE-IODINE 10% TOPICAL	Elevate Oral Care	27c29a33-d1cc-d72f-e063-6394a90a4d45	2025-09-19	Warnings	Exact identifier application number: M022
Povi-One	POVIDONE-IODINE 10% TOPICAL	Elevate Oral Care	f5252b4f-5e14-509e-e053-2995a90a6db8	2025-09-18	Warnings	Exact identifier application number: M022
Patterson Dental Topical Anesthetic	BENZOCAINE	Patterson Dental	3f199947-bf25-914b-e063-6394a90a8a6f	2025-09-18	Warnings	Exact identifier application number: M022
Patterson Dental Topical Anesthetic	BENZOCAINE	Patterson Dental	3f199947-bf28-914b-e063-6394a90a8a6f	2025-09-18	Warnings	Exact identifier application number: M022

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
L7T10EIP3A	MENTHOL, UNSPECIFIED FORM	1490-04-6	MENTHOL, UNSPECIFIED FORM

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
82939-001-01	82939000101	1 JAR in 1 PACKAGE (82939-001-01) > 4.2 g in 1 JAR	1 jar	2022-09-15	0000-00-00	No	No	Current
82939-001-02	82939000102	1 JAR in 1 BLISTER PACK (82939-001-02) / 7 g in 1 JAR	1 jar	2022-09-15		No	No	Current