Maximum Strength Medicated Foot Powder

Product NDC: 49035-795
Requested package NDC: 49035-795-01
11-digit product format: 490350795
Labeler code: 49035
Product ID: 49035-795_46f6ba22-d323-2610-e063-6394a90a486a
Type: HUMAN OTC DRUG
Nonproprietary name: Medicated Foot Powder
Dosage form: POWDER
Route: TOPICAL
Labeler: Walmart Stores Inc
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-09-01
Substance: MENTHOL
Active strength: .1 g/g
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: Maximum Strength Medicated Foot Powder
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	.1 g/g

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
259579	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
b0794d48-eb8b-55c9-e053-2995a90a5b38	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49035-795-01	Maximum Strength Medicated Foot Powder	283 g in 1 BOTTLE, PLASTIC	POWDER	283		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-795	MAXIMUM STRENGTH MEDICATED FOOT POWDER (MEDICATED FOOT POWDER) POWDER [WALMART STORES INC]	3	Current NDC, Legacy NDC, 1 package rows	20241220_b0794d48-eb8b-55c9-e053-2995a90a5b38.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 114 of 151 · 3,020 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Medicaine Sting and Bite	BENZOCAINE	James Alexander Corporation	753e6cbe-31e0-4017-93d0-8b4bf5972f37	2024-12-09	Warnings	Exact identifier application number: M017
AUVON Pain Relief Roll-on	MENTHOL	SHENZHEN YUWEN E-COMMERCE CO., LTD.	df239c4d-af6a-41ca-baed-d0788782ce9f	2024-12-08	Warnings	Exact identifier application number: M017
AUVON Pain Relief Roll-on	LIDOCAINE	SHENZHEN YUWEN E-COMMERCE CO., LTD.	8b30f623-6077-4f2e-8fa4-ce4a298953b5	2024-12-08	Warnings	Exact identifier application number: M017
QC Medicated anti itch	PRAMOXINE HYDROCHLORIDE, MENTHOL	Chain Drug Marketing Association	b5e41e3a-81df-3a63-e053-2a95a90a5839	2024-12-08	Warnings	Exact identifier application number: M017
QC Lidocaine Maximum Strength	LIDOCAINE HCL	Chain Drug Marketing Association	b5e1b1ab-8a95-2d2d-e053-2995a90aea53	2024-12-08	Warnings	Exact identifier application number: M017
Capsaicin	CAPSAICIN	Alexso, Inc	433da27d-04fb-481a-bbb0-874bb72c806a	2024-12-06	Warnings	Exact identifier application number: M017
POMG PAIN RELIEF BODY	LIDOCAINE	POMG LLC	28d7ac46-b27f-43bb-e063-6294a90a93ed	2024-12-06	Warnings	Exact identifier application number: M017
Capsaicin 0.1 Percent	CAPSAICIN	Alexso, Inc	0090ca38-6433-45c4-9453-edf2788c14c6	2024-12-06	Warnings	Exact identifier application number: M017
Signature Care Menthol	MENTHOL 4%	Safeway	27d3cb47-a6c7-5b7a-e063-6394a90a056f	2024-12-05	Warnings	Exact identifier application number: M017
ITCH X	BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE	BF ASCHER AND CO INC	03c16d33-8f59-0184-e054-00144ff8d46c	2024-12-05	Warnings	Exact identifier application number: M017
PO First Aid Series BURN	LIDOCAINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	f1c349a8-216d-4233-922e-c95329a33d1e	2024-12-05	Warnings	Exact identifier application number: M017
Post Treatment Balm	HYDROCORTISONE	Allure Labs Inc.	faa803e6-453c-4d86-85dd-5a5dcdd72d02	2024-12-05	Warnings	Exact identifier application number: M017
CBD Pain Relief Cream	TROLAMINE SALICYLATE	Allure Labs	b6b3102a-4154-2da2-e053-2995a90ae99f	2024-12-05	Warnings	Exact identifier application number: M017
CVS Health Pain Relieving	CAMPHOR (SYNTHETIC), MENTHOL (UNSPECIFIED FORM), METHYL SALICYLATE	Natural Essentials, Inc.	f7198485-3d68-41d2-b9b9-f932a0649310	2024-12-04	Warnings	Exact identifier application number: M017
Salonpas LIDOCAINE PLUS	BENZYL ALCOHOL, LIDOCAINE HYDROCHLORIDE	Hisamitsu America, Inc.	364924d3-fac3-4f4e-9b40-decd4ec48245	2024-12-03	Warnings	Exact identifier application number: M017
Bite and Itch	DIPHENHYDRAMINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE	Weeks & Leo Co., Inc.	0a4d471b-c3f3-0a6a-e063-6394a90ad57b	2024-12-03	Warnings	Exact identifier application number: M017
Menthol	AMISH ORIGINS MEDICATED	Amish Origins LLC	547abe39-3af3-4d70-99dd-caf8d67feda2	2024-12-03	Warnings	Exact identifier application number: M017
Meijer Small Cold-Hot Medicated Patches	MENTHOL	Meijer Distribution Inc	be6012d6-2062-45ba-8fc4-abf14cff5845	2024-12-03	Warnings	Exact identifier application number: M017
Salonpas	CAMPHOR, MENTHOL, METHYL SALICYLATE	Hisamitsu Pharmaceutical Co., Inc.	acdd5622-a9a7-4cc3-877e-57efea23303f	2024-12-03	Warnings	Exact identifier application number: M017
Salonpas	CAMPHOR, MENTHOL, METHYL SALICYLATE	Hisamitsu Pharmaceutical Co., Inc.	5bb6c6a3-7dc0-463d-ab2c-9f3bd3f3eff5	2024-12-03	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
259579	menthol 1 % Topical Powder	PSN	b0794d48-eb8b-55c9-e053-2995a90a5b38	4
259579	menthol 0.01 MG/MG Topical Powder	SCD	b0794d48-eb8b-55c9-e053-2995a90a5b38	4
259579	menthol 1 % Topical Powder	SY	b0794d48-eb8b-55c9-e053-2995a90a5b38	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49035-795-01	49035079501	283 g in 1 BOTTLE, PLASTIC (49035-795-01)	283 g	2020-09-01	0000-00-00	No	No	Current