Witch Hazel

Product NDC: 59779-045
11-digit product format: 597790045
Labeler code: 59779
Product ID: 59779-045_53c2fc99-1554-41ee-e063-6394a90a9efb
Type: HUMAN OTC DRUG
Nonproprietary name: Witch Hazel
Dosage form: LIQUID
Route: TOPICAL
Labeler: CVS Pharmacy, Inc.
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-04-04
Substance: WITCH HAZEL
Active strength: 860 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	59779-045	59779-045-99	D	Discontinued by firm		2026-10-12

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 · 18 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59779-045-99	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59779-045-99	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	59779-045-99	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	59779-045-99	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	59779-045-99	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	59779-045-99	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59779-045-99	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	59779-045-43	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59779-045-99	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	59779-045-43	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59779-045-99	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	59779-045-43	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59779-045-99	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	59779-045-43	`ad56d346431e…`	`cc804d4bbf1e…`

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: Witch Hazel
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
WITCH HAZEL	860 mg/mL

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
200295	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
50f920da-b41a-480d-b3a0-df940caaee2d	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-045-43	Witch Hazel	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		20
59779-045-99	Witch Hazel	236 mL in 1 BOTTLE, PUMP	LIQUID	236		20

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
WITCH HAZEL	ACTIVE INGREDIENT	101I4J0U34	WITCH HAZEL LIQUID [CVS PHARMACY]	1
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	WITCH HAZEL LIQUID [CVS PHARMACY]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	WITCH HAZEL LIQUID [CVS PHARMACY]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-045	WITCH HAZEL LIQUID [CVS PHARMACY]	19	Current NDC, Legacy NDC, 2 package rows	20250309_50f920da-b41a-480d-b3a0-df940caaee2d.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 13 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GoodSense Hemorrhoidal Pain Relief	GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL	Perrigo Direct, Inc	2e5f699d-45e8-6451-e063-6394a90a8ad8	2025-07-20	Warnings	Exact identifier application number: M015
Good Sense Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	L. Perrigo Company	379f8738-a871-4b09-abd1-c86386dfee04	2025-07-15	Warnings	Exact identifier application number: M015
Maximum Strength Hemorrhoidal Pads	WITCH HAZEL	Walmart, Inc.	6dd8d3d9-5109-4869-917b-9521e9ba1ed0	2025-07-14	Warnings	Exact identifier application number: M015
Nikzon Hemorrhoidal	GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, AND PRAMOXINE HYDROCHLORIDE	Genomma Lab USA	8f9a9939-2c99-489f-b597-9a51ec2684f9	2025-07-14	Warnings	Exact identifier application number: M015
ReVIVOL-XR	PHENYLEPHRINE HYDROCHLORIDE	Unipack LLC	2950fe83-a2a4-4ed4-b645-69d6fd2381ae	2025-07-13	Warnings	Exact identifier application number: M015
medicated wipes	WITCH HAZEL	Meijer Distribution Inc.	ba0f3f9a-95d1-4d8a-86d1-2c25c945118c	2025-07-11	Warnings	Exact identifier application number: M015
hemorrhoidal pads	WITCH HAZEL	Meijer Distribution Inc.	53e39d22-a89e-4f95-8c64-abeb50f72ce7	2025-07-11	Warnings	Exact identifier application number: M015
INVIGOR OH	LIDOCAINE	Natureplex LLC	7c7b536d-e41a-4017-9df9-982e2e9cfe4e	2025-07-10	Warnings	Exact identifier application number: M015
Maximum Strength Hemorrhoidal Cream with Aloe	GLYCERIN, PHENYLEPHINE HCI, PRAMOXINE HCI, PETROLATUM	Chain Drug Marketing Association	396ea654-8be1-591a-e063-6294a90a11e2	2025-07-08	Warnings	Exact identifier application number: M015
PREPARATION H SOOTHING RELIEF ANTI-ITCH	HYDROCORTISONE	Haleon US Holdings LLC	d6148d77-ef6f-4552-b5ba-43b429923f19	2025-07-07	Warnings	Exact identifier application number: M015
Rectal Care Cream	RECTAL CARE CREAM	Allegiant Health	ce585082-ad39-4b6f-a756-0d9a81a13eb8	2025-07-07	Warnings	Exact identifier application number: M015
Bisacodyl Laxative	BISACODYL LAXATIVE SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35cb0386-a662-6893-e063-6294a90aa71a	2025-07-03	Warnings	Exact identifier application number: M015
Hemorrhoidal Cream	GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM	Trifecta Pharmaceuticals Usa Llc	38cf4e43-280b-eb96-e063-6294a90a5949	2025-07-02	Warnings	Exact identifier application number: M015
TN Dickinsons Medicated Cooling Foam Hemorrhoidal Relief	WITCH HAZEL	Dickinson Brands Inc.	deca8ae2-53a3-4c90-aa10-45354e2cdab8	2025-06-27	Warnings	Exact identifier application number: M015
Glycerin Laxative	GLYCERIN LAXATIVE SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35cc266a-196f-16ce-e063-6394a90a24af	2025-06-20	Warnings	Exact identifier application number: M015
Phenylephrine Hemorrhoidal	HEMORRHOIDAL SUPPOSITORIES	Neilmed Pharmaceuticals Inc.	35ccb320-e902-3d1a-e063-6294a90a68d5	2025-06-20	Warnings	Exact identifier application number: M015
ProCure Hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Twin Med LLC	37a4cc43-0d53-f1bf-e063-6394a90a2dc9	2025-06-15	Warnings	Exact identifier application number: M015
Hemorrhoidal Pain Relief	HEMORRHOIDAL PAIN RELIEF OINTMENT	Neilmed Pharmaceuticals Inc.	374d89b6-9305-9adf-e063-6394a90adb32	2025-06-11	Warnings	Exact identifier application number: M015
Dermoplast Post Partum	BENZOCAINE	Advantice Health, LLC	374dced3-6527-b458-e063-6394a90a911e	2025-06-11	Warnings	Exact identifier application number: M015
foster and thrive hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	Strategic Sourcing Services LLC	fb3bc359-b06b-4995-aa68-0117a639dff2	2025-06-11	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
200295	witch hazel 86 % Topical Solution	PSN	50f920da-b41a-480d-b3a0-df940caaee2d	20
200295	witch hazel 860 MG/ML Topical Solution	SCD	50f920da-b41a-480d-b3a0-df940caaee2d	20
200295	witch hazel 86 % Topical Solution	SY	50f920da-b41a-480d-b3a0-df940caaee2d	20

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59779-045-43	59779004543	473 mL in 1 BOTTLE, PLASTIC (59779-045-43)	473 ml	2011-04-04	0000-00-00	No	No	Current
59779-045-99	59779004599	236 mL in 1 BOTTLE, PUMP (59779-045-99)	236 ml	2011-04-04	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
CVS 822.001/822AA Witch Hazel	CVS Pharmacy, Inc. \| Nice-Pak Products, LLC	2026-06-08	HUMAN OTC DRUG LABEL	21