Medicated Body Extra Strength

Product NDC: 49035-822
Requested package NDC: 49035-822-01
11-digit product format: 490350822
Labeler code: 49035
Product ID: 49035-822_46f6b8bd-9c3b-111b-e063-6394a90a7e2a
Type: HUMAN OTC DRUG
Nonproprietary name: MENTHOL 0.80%
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: 2.26 g/283g
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: Medicated Body Extra Strength
Brand name suffix: Powder
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
MENTHOL	2.26 g/283g

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
2169968	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
b0786418-7b28-d316-e053-2995a90a3ab5	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
49035-822-01	Medicated Body Extra StrengthPowder	283 g in 1 BOTTLE	POWDER	283		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49035-822	MEDICATED BODY EXTRA STRENGTH POWDER (MENTHOL 0.80%) POWDER [WALMART STORES INC]	3	Current NDC, Legacy NDC, 1 package rows	20241220_b0786418-7b28-d316-e053-2995a90a3ab5.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 60 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Diphenhydramine HCl and Zinc Acetate	EXTRA STRENGTH ITCH RELIEF	VALU MERCHANDISERS, CO	3e9c0f5b-cb76-475b-9a2b-39afa1eeb9ff	2025-11-24	Warnings	Exact identifier application number: M017
Menthol	MAXIMUM STRENGTH MEDICATED FOOT POWDER	VALU MERCHANDISERS, CO	89a5c4bb-442f-d3f0-e053-2a95a90a51bd	2025-11-24	Warnings	Exact identifier application number: M017
Dragon Pain Relieving Balm	CAMPHOR, MENTHOL	AMERICANNA WELLNESS, INC.	0d11ab8e-d3ea-c7ef-e063-6294a90ae0a3	2025-11-24	Warnings	Exact identifier application number: M017
Dragon Pain Relieving	CAMPHOR, MENTHOL	AMERICANNA WELLNESS, INC.	0d113dec-8832-d984-e063-6394a90ae7b3	2025-11-24	Warnings	Exact identifier application number: M017
Dragon Pain Relieving Balm	CAMPHOR, MENTHOL	AMERICANNA WELLNESS, INC.	0d12f03f-dd8b-0be5-e063-6294a90a43db	2025-11-24	Warnings	Exact identifier application number: M017
Thermacare Heat Therapy Max Strength Lidocaine Pain Relief Gel	THERMACARE HEAT THERAPY MAX STRENGTH LIDOCAINE PAIN RELIEF GEL	Clarion Brands LLC	445db02a-c8e8-6ebb-e063-6294a90a4301	2025-11-24	Warnings	Exact identifier application number: M017
Dragon Pain Relieving Balm	CAMPHOR, MENTHOL	AMERICANNA WELLNESS, INC.	0d129641-eaea-c3ee-e063-6394a90aa58f	2025-11-24	Warnings	Exact identifier application number: M017
Dragon Pain Relieving	CAMPHOR, MENTHOL	AMERICANNA WELLNESS, INC.	0d1059cc-1b0b-4e7b-e063-6294a90a56ea	2025-11-24	Warnings	Exact identifier application number: M017
GuruNanda Pain Relief	MENTHOL AND CAMPHOR	GURUNANDA, LLC	3ca78342-cc6d-5f6b-e063-6294a90a3f1c	2025-11-24	Warnings	Exact identifier application number: M017
Dragon Pain Relieving	CAMPHOR, MENTHOL	AMERICANNA WELLNESS, INC.	0d118256-90ee-28ef-e063-6394a90a21e8	2025-11-24	Warnings	Exact identifier application number: M017
health beyond	HYDROCORTISONE	Nantong Health & Beyond Hygienic Products Inc.	bdcd5b01-f5e2-4519-bf4d-25e3cc7e67af	2025-11-23	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches 3 Step	NICOTINE PATCHES	Shenzhen Paxi Trading Co., Ltd.	4429fea8-46f8-8f7f-e063-6394a90a34b4	2025-11-22	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches 2 Step	NICOTINE PATCHES	Shenzhen Paxi Trading Co., Ltd.	442a926b-d7c1-4e35-e063-6394a90ad948	2025-11-22	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches 1 Step	NICOTINE PATCHES	Shenzhen Paxi Trading Co., Ltd.	442aae32-4ac6-5dd6-e063-6294a90aad02	2025-11-22	Warnings	Exact identifier application number: M017
NicDuic Quit Smoking Nicotine Patches 1-3 Step	21MG NICOTINE PATCHES	Shenzhen Paxi Trading Co., Ltd.	442ae0fa-a1ed-7901-e063-6294a90ab717	2025-11-22	Warnings	Exact identifier application number: M017
IceQuake Lidocaine Analgesic	LIDOCAINE HYDROCHLORIDE	Dextrum Laboratories, Inc	441daa6f-f273-ac09-e063-6394a90a252c	2025-11-21	Warnings	Exact identifier application number: M017
Nighttime 4X Medicated Cream	BENZOCAINE	Rite Aid	21645ed1-2dc0-223a-e063-6394a90ab021	2025-11-21	Warnings	Exact identifier application number: M017
4x Medicated Gum Cream	BENZOCAINE	Albertsons	b81a308c-9c30-0e3d-e053-2a95a90a15d2	2025-11-21	Warnings	Exact identifier application number: M017
MENTHOL, CAMPHOR	MENTHOL, CAMPHOR	SUNSET NOVELTIES, INC	b0edd9d9-951f-d3dd-e053-2995a90a8d5a	2025-11-21	Warnings	Exact identifier application number: M017
Up up	LIDOCAINE PAIN RELIEF MAXIMUM STRENGTH PATCHES	Target Corporation	44121d40-86e1-0df6-e063-6294a90aedaf	2025-11-20	Warnings	Exact identifier application number: M017

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2169968	menthol 0.8 % Topical Powder	PSN	b0786418-7b28-d316-e053-2995a90a3ab5	4
2169968	menthol 0.008 MG/MG Topical Powder	SCD	b0786418-7b28-d316-e053-2995a90a3ab5	4
2169968	menthol 8 MG per GM Topical Powder	SY	b0786418-7b28-d316-e053-2995a90a3ab5	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49035-822-01	49035082201	283 g in 1 BOTTLE (49035-822-01)	283 g	2020-09-01	0000-00-00	No	No	Current