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		2026-10-16

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 6 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
AHLO PRO Healthy Gums	CETYLPYRIDINIUM CHLORIDE	Gervest USA Inc	4f5a0ccb-26e5-ebb6-e063-6394a90abbc5	2026-04-13	Warnings	Exact identifier application number: M022
Crest Scope Original Clean Mint	CETYLPYRIDINIUM CHLORIDE	The Procter & Gamble Manufacturing Company	4f1db6f4-acd7-a665-e063-6294a90a826b	2026-04-10	Warnings	Exact identifier application number: M022
Sore Throat	PHENOL GLYCERIN	Walgreens	1e845299-178e-49ce-9d08-7e9d548a5a6d	2026-04-09	Warnings	Exact identifier application number: M022
Sore throat cherry	PHENOL	Walgreens	67bed85e-e1e2-49ba-98d6-dfd4e1cd6856	2026-04-08	Warnings	Exact identifier application number: M022
Health-Tec Topical Anesthetic	BENZOCAINE	Dental Health Products, Inc.	5eb437c5-a2af-4c0d-b7b9-9ab7d093db85	2026-04-06	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	269b9e7f-c5c8-4023-a3ea-e39040ade271	2026-04-06	Warnings	Exact identifier application number: M022
Health-Tec Topical Anesthetic	BENZOCAINE	Dental Health Products, Inc.	c3fb6705-c647-4fe6-9aca-29735d01d8ea	2026-04-02	Warnings	Exact identifier application number: M022
Antiseptic	EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL	Family Dollar (FAMILY WELLNESS)	f061ec82-7f0e-4b93-afa6-ae9fe14ab4ea	2026-04-01	Warnings	Exact identifier application number: M022
CloSYS Silver Healthy Gums	CETYLPYRIDINIUM CHLORIDE	Rowpar Pharmaceuticals, Inc.	11fd3f31-ee0c-43d2-a856-929d1298277c	2026-04-01	Warnings	Exact identifier application number: M022
Crest Pro-Health Bold Fresh Breath	CETYLPYRIDINIUM CHLORIDE	The Procter & Gamble Manufacturing Company	5692c0ce-a914-08c4-e063-6394a90adf15	2026-04-01	Warnings	Exact identifier application number: M022
Anticavity Fluoride	SODIUM FLUORIDE AND ACIDULATED PHOSPHATE	Family Dollar (FAMILY WELLNESS)	1666fff6-9a8b-40f9-ae53-914152db386b	2026-04-01	Warnings	Exact identifier application number: M022
Sodium Chloride Normal Salt	SODIUM CHLORIDE	TWIN MED LLC	10230c8a-e5e5-44f1-b41d-80930899d6b9	2026-03-31	Warnings	Exact identifier application number: M022
Sootheez Birthday Cake	PECTIN	Primrose Candy Co.	4e5d8234-0521-0c8a-e063-6294a90ae62d	2026-03-31	Warnings	Exact identifier application number: M022
Sootheez Watermelon Mint	PECTIN	Primrose Candy Co.	4e5e4342-4647-ef25-e063-6394a90a1d13	2026-03-31	Warnings	Exact identifier application number: M022
PERIOGELX	HYDROGEN PEROXIDE	PERIO PROTECT, LLC	4e5a67a0-f989-50df-e063-6394a90aae73	2026-03-31	Warnings	Exact identifier application number: M022
Periogel	HYDROGEN PEROXIDE	PERIO PROTECT, LLC	1f9686b1-eac2-65b7-e063-6394a90a74fb	2026-03-31	Warnings	Exact identifier application number: M022
PERIOGELX	HYDROGEN PEROXIDE	PERIO PROTECT, LLC	1f7ecd75-bb59-2f4f-e063-6294a90ace84	2026-03-31	Warnings	Exact identifier application number: M022
Baza Protect	ZINC OXIDE AND DIMETHICONE	Coloplast Corp	ed63df26-3879-46df-8e09-10be569b25be	2026-03-31	Warnings	Exact identifier application number: M022
Benzocaine 20%	BENZOCAINE 20%	PAI Holdings, LLC dba PAI Pharma	7fbce9a5-00dc-4a4a-8709-ab752bdf2f59	2026-03-25	Warnings	Exact identifier application number: M022
Kroger Extra Whitening	FLUORIDE	Kroger	e704c690-1383-4cd6-be85-28bdd9ff936b	2026-03-24	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