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 9 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CVS Hemorrhoidal Lidocaine 5 Rapid Pain Relief with 10 Finger Cots	LIDOCAINE	CVS PHARMACY, INC	caef51a8-76e9-42b3-a160-c54f62b47de1	2026-01-05	Warnings	Exact identifier application number: M015
CVS Maximum OTC Strength Hemorrhoidal with Aloe	GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, WHITE PETROLATUM	CVS PHARMACY,INC	b55c63fb-5dfa-4567-8192-58f403868837	2026-01-02	Warnings	Exact identifier application number: M015
HemRid Anorectal Cream	LIDOCAINE	KKA & Associates LLC	dbeb4325-3e85-1147-e053-2995a90a2160	2025-12-31	Warnings	Exact identifier application number: M015
ElixirCurozole	CLOTRIMAZOLE	ELIXIR HEALTHCARE USA, LLC.	0c468a9e-d092-4704-b742-92ecd9918209	2025-12-26	Warnings	Exact identifier application number: M015
Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HYDROCHLORIDE	GRAXCELL PHARMACEUTICAL, LLC	5162baee-0d63-494e-8046-459437b85348	2025-12-25	Warnings	Exact identifier application number: M015
HEMORRHOIDAL	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE	Safeway	3e6728b6-26e3-4287-8ba6-e27f305cd93b	2025-12-20	Warnings	Exact identifier application number: M015
PREPARATION H	PHENYLEPHRINE HYDROCHLORIDE	Haleon US Holdings LLC	40fde50a-3cc0-4286-9b33-8f3912254c33	2025-12-18	Warnings	Exact identifier application number: M015
ElixirLidoFast Rapid Relief	GLYCERIN, LIDOCAINE, PETROLATUM, AND PHENYLEPHRINE HYDROCHLORIDE	ELIXIR HEALTHCARE USA, LLC.	45de9dfa-6c89-1eae-e063-6294a90a4dac	2025-12-13	Warnings	Exact identifier application number: M015
topcare hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	Topco Associates LLC	81a3546b-5099-4b9a-b774-b3e79316b267	2025-12-13	Warnings	Exact identifier application number: M015
Kroger Hemorrhoid	GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL	Kroger Company	45b2dd86-7fb0-07bf-e063-6394a90a1884	2025-12-11	Warnings	Exact identifier application number: M015
LMX5	LIDOCAINE	Ferndale Laboratories, Inc.	34f8ed6b-4a52-4a99-9c1b-254196dc29b0	2025-12-10	Warnings	Exact identifier application number: M015
PURA	WITCH HAZEL	Mypura.com Limited	1523f52f-6a5b-a12d-e063-6294a90a4496	2025-12-05	Warnings	Exact identifier application number: M015
Menthol and Zinc Oxide	MENTHOL AND ZINC OXIDE	Marlex Pharmaceuticals, Inc.	c24e2dab-cab4-38f4-e053-2995a90aabae	2025-12-04	Warnings	Exact identifier application number: M015
CAREALL Hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	New World Imports, Inc	7913bd41-a606-4ca6-b69f-2717c2f54b07	2025-12-01	Warnings	Exact identifier application number: M015
Dr Butlers Hemorrhoid and Fissure PF	LIDOCAINE 4.00, PHENYLEPHRINE HYDROCHLORIDE 0.25	Beyond Health P.A.	f526199e-5c9e-7a3c-e053-2a95a90aa98e	2025-11-26	Warnings	Exact identifier application number: M015
Meicated Wipe	WITCH HAZEL	Diamond Wipes International, Inc	4458c80c-d013-55ba-e063-6394a90a6b39	2025-11-24	Warnings	Exact identifier application number: M015
Hemorrhoidal Cream	GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM	Trifecta Pharmaceuticals Usa Llc	804d7b1f-1be8-50c9-e053-2a91aa0a35d0	2025-11-18	Warnings	Exact identifier application number: M015
Launch Medical	LIDOCAINE HYDROCHLORIDE	Sambria Pharmaceuticals, LLC	293ef514-44c1-43ac-9a81-c30e34ad39e5	2025-11-12	Warnings	Exact identifier application number: M015
FARGELIN HEMORRHOIDAL	CALAMINE, PETROLATUM AND PHENYLEPHRINE HYDROCHLORIDE	MADISON ONE ACME INC	6844ad63-512d-496a-9458-011894185b0d	2025-11-10	Warnings	Exact identifier application number: M015
Hazel Perineal Healing Foam	WITCH HAZEL	Jiangsu Senwo Medical Technology Co., Ltd.	314b75cb-affe-a248-e063-6294a90a47b7	2025-11-07	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