Point Relief Cold Spot Pain Relieving

Product NDC: 51452-035
Requested package NDC: 51452-035-01
11-digit product format: 514520035
Labeler code: 51452
Product ID: 51452-035_0fc4ec9e-6c21-5a8c-e063-6394a90a11ef
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: GEL
Route: TOPICAL
Labeler: Fabrication Enterprises
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-04-01
Substance: MENTHOL
Active strength: 120 mg/mL
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	51452-035	51452-035-01	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 · 12 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…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: Point Relief Cold Spot Pain Relieving
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	120 mg/mL

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 RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2121666	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
ad5d6f04-15e6-4548-95c2-32271c186bc1	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51452-035-01	Point Relief Cold Spot Pain Relieving	120 mL in 1 BOTTLE	GEL	120	4
51452-035-02	Point Relief Cold Spot Pain Relieving	475 mL in 1 BOTTLE	GEL	475	4
51452-035-03	Point Relief Cold Spot Pain Relieving	3800 mL in 1 JUG	GEL	3800	4
51452-035-04	Point Relief Cold Spot Pain Relieving	420 mL in 1 TUBE	GEL	420	4
51452-035-05	Point Relief Cold Spot Pain Relieving	950 mL in 1 BOTTLE	GEL	950	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51452-035	POINT RELIEF COLD SPOT PAIN RELIEVING (MENTHOL) GEL [FABRICATION ENTERPRISES]	4	Current NDC, Legacy NDC, 5 package rows	20240126_ad5d6f04-15e6-4548-95c2-32271c186bc1.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 51 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PREMIERES PAIN	MENTHOL	Premiere Enterprises	35ff19df-4cc4-4fce-bd30-d87d835e0e26	2025-12-23	Warnings	Exact identifier application number: M017
Premieres Pain	MENTHOL	Premiere Enterprises	1f081913-6106-4d06-a37a-631f710dbacb	2025-12-23	Warnings	Exact identifier application number: M017
ABSORBINE jr.	LIDOCAINE HCL, PHENOL	Clarion Brands, LLC	e1de73bb-917c-48d1-9a78-00c76edddb98	2025-12-23	Warnings	Exact identifier application number: M017
ABSORBINE jr. PLUS Knee	CAMPHOR, MENTHOL	Clarion Brands, LLC	3ad8718d-ebf1-474f-8a91-48c78ab3b5c1	2025-12-23	Warnings	Exact identifier application number: M017
Absorbine Jr. Plus	MENTHOL	Clarion Brands, LLC	fd5d77fc-dc73-2aec-2c7f-0fca5d7d3a75	2025-12-23	Warnings	Exact identifier application number: M017
ABSORBINE JR PLUS ULTRA STRENGTH PAIN	MENTHOL	Clarion Brands, LLC	cf329707-d90a-29dd-f2c2-acfd5af614f3	2025-12-23	Warnings	Exact identifier application number: M017
Absorbine Jr Pro Cream	LIDOCAINE HCL, PHENOL	Clarion Brands, LLC	17b3f1e6-5554-4f3e-b133-76ae8ffea919	2025-12-23	Warnings	Exact identifier application number: M017
Absorbine Jr Pro No Mess Roll-on Plus	LIDOCAINE HCL, PHENOL	Clarion Brands, LLC	a7172f17-1525-4738-b72c-92479c730af2	2025-12-23	Warnings	Exact identifier application number: M017
ABSORBINE JR	MENTHOL	Clarion Brands, LLC	d656e7f6-ca26-1873-6c11-08aa82091bb0	2025-12-23	Warnings	Exact identifier application number: M017
Relief Recovery	METHYL SALICYLATE	Mayway Corporation	27afd45e-2dc5-d099-e063-6394a90ad2b7	2025-12-23	Warnings	Exact identifier application number: M017
Mobility	METHYL SALICYLATE	Mayway Corporation	27af9d17-9c15-5e2a-e063-6394a90aeda5	2025-12-23	Warnings	Exact identifier application number: M017
medlot pain relief gel patch	LIDOCAINE	Lotfancy, Inc.	3ce4af20-b227-5b98-e063-6394a90ab992	2025-12-23	Warnings	Exact identifier application number: M017
Nizoral Scalp Itch Relief	HYDROCORTISONE	Kramer Laboratories	dba59238-6beb-447e-8c4c-e4bc00fd2c20	2025-12-23	Warnings	Exact identifier application number: M017
Salonpas LIDOCAINE Pain Relieving	LIDOCAINE	Hisamitsu America, Inc.	63911880-8194-4c7d-a72f-cab94761b2d7	2025-12-23	Warnings	Exact identifier application number: M017
The Body Builders Cream	MENTHOL	Smart Cookie Solutions	f803325e-eb86-4b9e-a401-0a91bdcd6389	2025-12-22	Warnings	Exact identifier application number: M017
PROINNATE Numbing Cream	LIDOCAINE,MENTHOL	Guangdong Aimu Biological Technology Co., Ltd	46895ddb-0b9f-675e-e063-6394a90adf23	2025-12-22	Warnings	Exact identifier application number: M017
Caring Mills Vaginal Anti-Itch Cream	BENZOCAINE, RESORCINOL	Veridian Healthcare	f2362658-aea2-438e-a66c-738022e6e047	2025-12-22	Warnings	Exact identifier application number: M017
HealthWise Pain Relieving Menthol Gel	MENTHOL 2%	Veridian Healthcare	396d0fd4-67be-4de1-8f0c-42c83dfe9120	2025-12-22	Warnings	Exact identifier application number: M017
Large Medicate Relief Patches	CAMPHOR, MENTHOL, METHYL SALICYLATE	Amerisource Bergen	a7d5f89b-59b9-4603-99aa-273b85be813e	2025-12-22	Warnings	Exact identifier application number: M017
Good Neighbor Capsaicin Heat Patch for Back	CAPSAICIN	Amerisource Bergen	f873a0b8-8123-1600-e053-6394a90a043e	2025-12-22	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2121666	menthol 0.12 MG/MG Topical Gel	PSN	ad5d6f04-15e6-4548-95c2-32271c186bc1	4
2121666	menthol 0.12 MG/MG Topical Gel	SCD	ad5d6f04-15e6-4548-95c2-32271c186bc1	4
2121666	menthol 12 % Topical Gel	SY	ad5d6f04-15e6-4548-95c2-32271c186bc1	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
51452-035-01	51452003501	120 mL in 1 BOTTLE (51452-035-01)	120 ml	2019-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Point Relief Cold Spot Pain Relieving Gel	Fabrication Enterprises	2024-01-25	HUMAN OTC DRUG LABEL	4