medicated wipes

Product NDC: 41250-988
11-digit product format: 412500988
Labeler code: 41250
Product ID: 41250-988_39ad5009-370b-0d4b-e063-6294a90ad1bf
Type: HUMAN OTC DRUG
Nonproprietary name: Witch Hazel
Dosage form: PATCH
Route: TOPICAL
Labeler: Meijer Distribution Inc.
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-06-28
Substance: WITCH HAZEL
Active strength: 500 mg/1000mg
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41250-988-48	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	41250-988-96	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41250-988-48	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	41250-988-96	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41250-988-48	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	41250-988-96	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	41250-988-48	`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	41250-988-96	`8dfbde2a14a4…`	`c9ff85d89658…`

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 wipes
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
WITCH HAZEL	500 mg/1000mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
101I4J0U34	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
844379	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
ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
41250-988-48	2022-12-19	Drug Facts
41250-988-96	2022-12-19	Drug Facts
41250-988-48	2021-01-29	Drug Facts
41250-988-96	2021-01-29	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
41250-988-48	medicated wipes	500 mg in 1 PATCH	PATCH	500	4
41250-988-48	medicated wipes	48 in 1 BOX	PATCH	48	4
41250-988-96	medicated wipes	500 mg in 1 PATCH	PATCH	500	4
41250-988-96	medicated wipes	96 in 1 BAG	PATCH	96	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-988	MEDICATED WIPES (WITCH HAZEL) PATCH [MEIJER DISTRIBUTION INC.]	3	Current NDC, Legacy NDC, 4 package rows	20240113_ba0f3f9a-95d1-4d8a-86d1-2c25c945118c.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 11 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Medline	MENTHOL, WHITE PETROLATUM, ZINC OXIDE	Medline Industries, LP	006539c9-1982-d6de-e063-6294a90a1a5a	2025-10-17	Warnings	Exact identifier application number: M015
Xesso Strawberry Rear Comfort Glide 4% Lidocaine	LIDOCAINE	Premium Natural Cosmetics Inc	efba09fc-6dd7-0f73-e053-2995a90a628a	2025-10-17	Warnings	Exact identifier application number: M015
medicated pads	WITCH HAZEL	TARGET CORPORATION	acd0d99d-2a77-4227-bebb-c819f4a52666	2025-10-14	Warnings	Exact identifier application number: M015
Acolye Numbing Cream Anorectal(Hemorrhoidal) Cream	LIDOCAINE	Guangzhou Haishi Biological Technology Co., Ltd.	40b0e8d6-4686-960b-e063-6294a90a016e	2025-10-09	Warnings	Exact identifier application number: M015
Acolye Numbing Cream Anorectal(Hemorrhoidal) Cream	LIDOCAINE	Guangzhou Haishi Biological Technology Co., Ltd.	40b452a3-76b7-2433-e063-6294a90ab6b4	2025-10-09	Warnings	Exact identifier application number: M015
EQUATE HEMORRHOID RELIEF	LIDOCAIN 5%	WALMART, INC	d96e8152-e36e-22fc-e053-2995a90a8b2b	2025-10-08	Warnings	Exact identifier application number: M015
Pramoxine Hydrochloride Anorectal	PRAMOXINE HYDROCHLORIDE	Stratus Pharmaceuticals	39a16b66-b0e9-412f-8773-8dec0a1227e0	2025-10-02	Warnings	Exact identifier application number: M015
Doctor Butlers Hemorrhoid and Fissure External Pain Formula	LIDOCAINE 5%	Beyond Health, P.A.	d92f22a7-c0b5-d8b8-e053-2a95a90a2376	2025-09-30	Warnings	Exact identifier application number: M015
RWWXII Deep Numbing Cream(Anorectal Hemorrhoidal Cream)	LIDOCAINE	Guangzhou Haishi Biological Technology Co., Ltd.	3ffc57c7-5bf4-cba8-e063-6394a90a322f	2025-09-29	Warnings	Exact identifier application number: M015
Hemorrhoidal Pain Relief	HEMORRHOIDAL PAIN RELIEF CREAM	Neilmed Pharmaceuticals Inc.	374dc1c0-4243-b272-e063-6394a90a5a6b	2025-09-24	Warnings	Exact identifier application number: M015
Medi-First Burn	LIDOCAINE HYDROCHLORIDE	Unifirst First Aid Corporation	44bb5f25-1114-4bb1-8bcf-40402594abc4	2025-09-09	Warnings	Exact identifier application number: M015
Dr. Care Numbing Cream	5% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	3e456af7-9726-d17e-e063-6394a90ab560	2025-09-08	Warnings	Exact identifier application number: M015
Medi-first Ivy-Rid First Aid	BENZOCAINE AND BENZETHONIUM CHLORIDE	Unifirst First Aid Corporation	905c97ad-0bba-46b1-939c-f16fbdb02818	2025-09-08	Warnings	Exact identifier application number: M015
MediFirst Burn	LIDOCAINE HYDROCHLORIDE	Unifirst First Aid Corporation	9fa5b348-29c2-4cd0-a945-0486bd27f5e0	2025-09-08	Warnings	Exact identifier application number: M015
Medi-First Burn	LIDOCAINE HCL	Unifirst First Aid Corporation	b3ebf104-cc51-0ef5-e053-2a95a90a25c9	2025-09-08	Warnings	Exact identifier application number: M015
Lidocaine Hydrochloride	LIDOCAINE HYDROCHLORIDE	Unifirst First Aid Corporation	4c2e2b91-d2f6-4e41-9a4c-ecabca9830e8	2025-09-08	Warnings	Exact identifier application number: M015
Pain Relief	ANALGESIC MENTHOL	Unifirst First Aid Corporation	8162d22d-04c0-de07-e053-2991aa0a9975	2025-09-08	Warnings	Exact identifier application number: M015
Green Guard Burn	LIDOCAINE HCL	Unifirst First Aid Corporation	b451e96f-fcba-6495-e053-2a95a90a2adf	2025-09-08	Warnings	Exact identifier application number: M015
Lidochill(TM) Gel	LIDOCAINE HCL 4%, MENTHOL 1%	PureTek Corporation	d2a9aeb6-8a94-49e7-ab46-84403560b6c8	2025-09-08	Warnings	Exact identifier application number: M015
Signature numbing cream	5% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	3e1892de-378b-d2d0-e063-6294a90ad7db	2025-09-05	Warnings	Exact identifier application number: M015

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
101I4J0U34	WITCH HAZEL	WITCH HAZEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
844379	witch hazel 50 % Medicated Pad	PSN	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	4
844379	witch hazel 500 MG/ML Medicated Pad	SCD	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	4
844379	witch hazel 50 % Medicated Pad	SY	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	4
844379	witch hazel 50 % Medicated Wipes	SY	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-988-48	41250098848	48 PATCH in 1 BOX (41250-988-48) / 500 mg in 1 PATCH	48 patch	2019-10-02	0000-00-00	No	No	Current
41250-988-96	41250098896	96 PATCH in 1 BAG (41250-988-96) / 500 mg in 1 PATCH	96 patch	2019-10-02	0000-00-00	No	No	Current