SUPER WHITE STUFF PAIN RELIEF

Product NDC: 14448-315
11-digit product format: 144480315
Labeler code: 14448
Product ID: 14448-315_09d6fabb-0d2a-222e-e063-6294a90a95b6
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL
Dosage form: CREAM
Route: TOPICAL
Labeler: BLUE SPRING WELLNESS, L.L.C.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-04-19
Substance: MENTHOL
Active strength: 14 mg/mL
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: SUPER WHITE STUFF PAIN RELIEF
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	14 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
2391332	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
b4278b70-e9a6-4d1f-bbad-257fe437b86a	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
14448-315-00	SUPER WHITE STUFF PAIN RELIEF	5 mL in 1 PACKET	CREAM	5		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
14448-315	SUPER WHITE STUFF PAIN RELIEF (MENTHOL) CREAM [BLUE SPRING WELLNESS, L.L.C.]	3	Current NDC, Legacy NDC, 1 package rows	20231111_b4278b70-e9a6-4d1f-bbad-257fe437b86a.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 55 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ElixirLidoFast	LIDOCAINE 5% CREAM	ELIXIR HEALTHCARE USA, LLC.	45de5a3d-06c2-aa02-e063-6294a90a63d3	2025-12-13	Warnings	Exact identifier application number: M017
MEDI FIRST PLUS	HYDROCORTISONE ACETATE	Orazen Inc	5781124a-60f4-4a64-80b7-ce5f28d495b5	2025-12-12	Warnings	Exact identifier application number: M017
MEDI-FIRST	HYDROCORTISONE ACETATE	Orazen Inc	aeffd85c-58a7-4d64-bf94-977b6fbbe713	2025-12-12	Warnings	Exact identifier application number: M017
Joint and Muscle Relief	MENTHOL	Smart Cookie Solutions Inc.	45c24d56-4dc9-2884-e063-6294a90a52cc	2025-12-12	Warnings	Exact identifier application number: M017
Popstar	DELAY SPRAY	Pineapple Brands LLC	293b2da9-1261-0358-e063-6394a90aa08c	2025-12-12	Warnings	Exact identifier application number: M017
Careland Pain Relief Plus	CAMPHOR, MENTHOL, METHYL SALICYLATE	Planet (Anhui) Pharmaceutical Co., Ltd.	d9e63ddd-d003-45fa-b156-7f4452c28cbd	2025-12-12	Warnings	Exact identifier application number: M017
Glucosamine Cream EXTRA STRENGTH	HISTAMINE DIHYDROCHLORIDE	IDEAZ, LLC	f4d414b7-89e7-ad65-e053-2a95a90a25d4	2025-12-12	Warnings	Exact identifier application number: M017
ARTHRITIS	MENTHOL	Smith Amish, LLC	20c36972-b695-1241-e063-6394a90adf63	2025-12-12	Warnings	Exact identifier application number: M017
FOOT	MENTHOL	Smith Amish, LLC	20c48537-f55f-c10f-e063-6394a90a4cca	2025-12-12	Warnings	Exact identifier application number: M017
Joint Ease	MENTHOL	Smith Amish, LLC	20c4a0f8-bdc6-d89a-e063-6294a90aa8d8	2025-12-12	Warnings	Exact identifier application number: M017
Toast Screamin Hot	CAPSAICIN	IDEAZ, LLC	331207e6-b8ac-b169-e063-6394a90ac169	2025-12-12	Warnings	Exact identifier application number: M017
Pain Relief Gel-Patch	LIDOCAINE	KORVIA GLOBAL Inc.	45ccfcae-a307-1c5f-e063-6294a90acf89	2025-12-12	Warnings	Exact identifier application number: M017
Lidospot patch	LIDOCAINE AND MENTHOL	Fabrication Enterprises Inc	3a6e94c4-1ca6-e77a-e063-6394a90a4bfc	2025-12-12	Warnings	Exact identifier application number: M017
LETEBEE LIGHT neuropathy pain relief cream for feet	MENTHOL	Guangdong Aimu Biological Technology Co., Ltd	45a99afc-15ec-76c2-e063-6294a90a2220	2025-12-11	Warnings	Exact identifier application number: M017
Cinthera	LIDOCAINE	Strand Health Group	2746e5b2-be2d-f2d2-e063-6394a90a3690	2025-12-11	Warnings	Exact identifier application number: M017
Equate Cool and Heat Pain Relieving Liquid	COOL AND HEAT PAIN RELIEF	Walmart, Inc.	ad156685-3bd5-6837-e053-2995a90ac788	2025-12-11	Warnings	Exact identifier application number: M017
HUMCO Camphor Spirit	CAMPHOR 10%	Humco Holding Group, Inc.	9a0ef0a3-3c79-41b2-8193-424a3ef9886f	2025-12-11	Warnings	Exact identifier application number: M017
T-Relief Lidocaine HCL 4%	LIDOCAINE HCL 4%	Medinatura New Mexico Inc.	3c19aff8-fb18-78d0-e063-6294a90a9481	2025-12-11	Warnings	Exact identifier application number: M017
Jointiva	TROLAMINE SALICYLATE 10%	Rising Pharma Holdings, Inc.	3ee33cbf-7c0f-4982-b0b6-eeeb0202803b	2025-12-11	Warnings	Exact identifier application number: M017
LMX4	LIDOCAINE	Ferndale Laboratories, Inc.	f0e7c92f-8b0b-4045-b659-af9f6e81260f	2025-12-10	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2391332	menthol 1.4 % Topical Cream	PSN	b4278b70-e9a6-4d1f-bbad-257fe437b86a	3
2391332	menthol 14 MG/ML Topical Cream	SCD	b4278b70-e9a6-4d1f-bbad-257fe437b86a	3
2391332	menthol 1.4 % Topical Cream	SY	b4278b70-e9a6-4d1f-bbad-257fe437b86a	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
14448-315-00	14448031500	5 mL in 1 PACKET (14448-315-00)	5 ml	2021-04-19	0000-00-00	No	No	Current