Still Standing

Product NDC: 66902-167
11-digit product format: 669020167
Labeler code: 66902
Product ID: 66902-167_4c0f6b65-79d8-db14-e063-6394a90aaeb9
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL, UNSPECIFIED FORM
Dosage form: LIQUID
Route: TOPICAL
Labeler: Natural Essentials Inc.
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-02-28
Substance: MENTHOL, UNSPECIFIED FORM
Active strength: 100 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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: Still Standing
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	100 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
667889	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
66974aaf-c82f-4fe9-bfb3-3430b80ac9f2	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
66902-167-15	Still Standing	15 mL in 1 BOTTLE, SPRAY	LIQUID	15	4
66902-167-17	Still Standing	15 mL in 1 BOTTLE, SPRAY	LIQUID	15	4
66902-167-18	Still Standing	18 mL in 1 BOTTLE, SPRAY	LIQUID	18	4
66902-167-34	Still Standing	100 mL in 1 BOTTLE, SPRAY	LIQUID	100	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66902-167	STILL STANDING (MENTHOL, UNSPECIFIED FORM) LIQUID [NATURAL ESSENTIALS INC.]	2	Current NDC, 4 package rows	20241006_66974aaf-c82f-4fe9-bfb3-3430b80ac9f2.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 29 of 156 · 3,115 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Topicaine Ultra	TOPICAINE ULTRA	Oncora Pharma, LLC	e052f718-700a-44e0-8770-65451b812ee1	2026-03-24	Warnings	Exact identifier application number: M017
Hot Pap Cataplasma	METHYL SALICYLATE, VANILLYL NONYLAMIDE	Masaem Company	4dbeda13-b198-0cf0-e063-6294a90a8180	2026-03-24	Warnings	Exact identifier application number: M017
Nervive Pain Relieving Cream	LIDOCAINE HCL AND MENTHOL	The Procter & Gamble Manufacturing Company	1e8bfb1e-8f5a-d0f3-e063-6294a90a752a	2026-03-24	Warnings	Exact identifier application number: M017
Nervive Pain Relieving Liquid Roll-on	LIDOCAINE HCL AND MENTHOL	The Procter & Gamble Manufacturing Company	1e8aeccc-8d00-9886-e063-6394a90ad7a6	2026-03-24	Warnings	Exact identifier application number: M017
Nervive Pain Relieving	LIDOCAINE HCL AND MENTHOL	The Procter & Gamble Manufacturing Company	32f8d0f3-d18d-1a45-e063-6294a90a6ad3	2026-03-24	Warnings	Exact identifier application number: M017
BARMICIL PLUS	HYDROCORTISONE	OPMX LLC	fb5f4743-61e8-46c8-8561-38e17aeaa4d5	2026-03-24	Warnings	Exact identifier application number: M017
Barmicil Anti-itch	HYDROCORTISONE	OPMX LLC	850084c3-1dd4-eb8d-e053-2a91aa0a130b	2026-03-24	Warnings	Exact identifier application number: M017
Jeil Hangbang Paff Soo S Cataplasma	GLYCOL SALICYLATE, L-MENTHOL	Masaem Company	4dd040db-07cf-361a-e063-6394a90a8001	2026-03-24	Warnings	Exact identifier application number: M017
Zenol Double Action	METHYL SALICYLATE, L-MENTHOL	BA TRADE INC	4da998fc-75a3-583f-e063-6394a90a59c7	2026-03-23	Warnings	Exact identifier application number: M017
Ultra Strength Topical Pain Relief Cream	CAMPHOR, MENTHOL, METHYL SALICYLATE	J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD	4db9ae57-4ab4-8fe4-e063-6394a90a7e51	2026-03-23	Warnings	Exact identifier application number: M017
DR. SANA ALIVIO TOTAL ALIVIO TOTAL ROLL ON	ALIVIO TOTAL ROLL ON	EVI LABS	4da01338-8739-08a8-e063-6294a90ae157	2026-03-22	Warnings	Exact identifier application number: M017
DR SANA ALIVIO TOTAL ALIVIO TOTAL	ALIVIO TOTAL	EVI LABS	4da1c3b8-9af2-6e9f-e063-6394a90a86ae	2026-03-22	Warnings	Exact identifier application number: M017
SORE NO MORE	MENTHOL CAMPHOR	SOMBRA COSMETICS INC.	80d97c80-bdc0-4d5d-b6e2-86dfdb15d7bd	2026-03-20	Warnings	Exact identifier application number: M017
CVS Health Antiseptic Wound Wash	LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE	CVS Pharmacy	53ac017a-eccb-3b24-e054-00144ff88e88	2026-03-20	Warnings	Exact identifier application number: M017
Tecnu Diphenhydramine HCl Pain Relieving Anti Itch Gel 2%	ANTI ITCH GEL	Walgreens	3d6e8c62-2fcc-51c2-e063-6394a90a33f7	2026-03-20	Warnings	Exact identifier application number: M017
ANIXIKE Numbing	MENTHOL 5% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4d5c52d7-8e81-b62f-e063-6394a90ad03e	2026-03-19	Warnings	Exact identifier application number: M017
Vicks VapoFreeze PAIN RELIEVING	CAMPHOR, MENTHOL	The Procter & Gamble Manufacturing Company	4038e50d-b53b-4f56-b54e-62157e286e08	2026-03-19	Warnings	Exact identifier application number: M017
Vicks VapoFreeze PAIN RELIEVING	CAMPHOR, MENTHOL	The Procter & Gamble Manufacturing Company	a8a550d8-55d0-4a0b-b4c0-5d64f0227895	2026-03-19	Warnings	Exact identifier application number: M017
SYLVIRENE NUMBING	MENTHOL 5% NUMBING	Jiangxi Yudexi Pharmaceutical Co., LTD	4d47e8c7-d293-bf63-e063-6294a90a5fd9	2026-03-18	Warnings	Exact identifier application number: M017
Antibiotic and Pain Relief	NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE	STRATEGIC SOURCING SERVICES LLC	f7aa9330-c47c-4d2f-b784-11b831d919d6	2026-03-18	Warnings	Exact identifier application number: M017

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
667889	menthol 10 % Topical Spray	PSN	66974aaf-c82f-4fe9-bfb3-3430b80ac9f2	4
667889	menthol 100 MG/ML Topical Spray	SCD	66974aaf-c82f-4fe9-bfb3-3430b80ac9f2	4
667889	menthol 10 % Topical Spray	SY	66974aaf-c82f-4fe9-bfb3-3430b80ac9f2	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
66902-167-15	66902016715	15 mL in 1 BOTTLE, SPRAY (66902-167-15)	15 ml	2023-02-28	No	No	Current
66902-167-17	66902016717	15 mL in 1 BOTTLE, SPRAY (66902-167-17)	15 ml	2023-02-28	No	No	Current
66902-167-18	66902016718	18 mL in 1 BOTTLE, SPRAY (66902-167-18)	18 ml	2023-02-28	No	No	Current
66902-167-34	66902016734	100 mL in 1 BOTTLE, SPRAY (66902-167-34)	100 ml	2026-03-02	No	No	Current