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		2026-10-05

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 6 of 23 · 441 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PREPARATION H MEDICATED WIPES	WITCH HAZEL	Haleon US Holdings LLC	8d9961f0-1ecf-d7fb-b6b4-856d636d68e1	2026-03-17	Warnings	Exact identifier application number: M015
Crane Safety Burn	LIDOCAINE	Crane Safety LLC	96d81566-6321-731e-e053-2995a90ad07d	2026-03-16	Warnings	Exact identifier application number: M015
Signature Lidocaine Pain Relief Cream	5% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	4c56b3b3-33b3-a50e-e063-6394a90a955f	2026-03-06	Warnings	Exact identifier application number: M015
WowDay Medicated Hemorrhoidal Flushable Wipes	MEDICATED HEMORRHOIDAL FLUSHABLE WIPES	WowDay LLC	4c603b27-4835-bc40-e063-6394a90a8ea2	2026-03-06	Warnings	Exact identifier application number: M015
Numb Fast Hemorrhoidal	LIDOCAINE	Oasis Plus LLC	a00ffed7-8034-4cc0-87c4-3c793c1bcd6e	2026-03-03	Warnings	Exact identifier application number: M015
Curist Lidocaine Relief	LIDOCAINE 5%	Little Pharma, Inc.	f562b57d-6592-93fa-e053-2995a90ae3e0	2026-03-02	Warnings	Exact identifier application number: M015
Therapain Plus	MENTHOL ROLL-ON	Epic Laboratories, LLC	0249cfdf-b7c4-f27d-e063-6294a90aaa26	2026-03-02	Warnings	Exact identifier application number: M015
Liposomal Hemorrhoid Master	LIDOCAINE , PHENYLEPHRINE HCL	Clinical Resolution Laboratory, Inc.	a1e15d2a-44b6-4d9c-89c2-0ff12285724e	2026-03-02	Warnings	Exact identifier application number: M015
Equate Hemorrhoid Relief	LIDOCAINE	Walmart Inc.	48646860-ed5d-62a0-e063-6394a90abb23	2026-03-01	Warnings	Exact identifier application number: M015
Witch Hazel	WITCH HAZEL	The Kroger Co.	bbf2efd7-f181-403b-ac5f-695f7ba15875	2026-02-27	Warnings, Adverse reactions	Exact identifier application number: M015
Dermatool Hemorrhoidal	GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL	Papalo Group LLC	4bc06f41-7733-ebd0-e063-6294a90af7a8	2026-02-26	Warnings	Exact identifier application number: M015
Megababe Fun Gal Stuff Antifungal	CLOTRIMAZOLE	Megababe LLC	c599d27b-fdb0-465f-9e43-13d32c520a92	2026-02-25	Warnings	Exact identifier application number: M015
Witch Hazel	WITCH HAZEL	Better Living Brands, LLC	0355edab-b6f7-4e59-bce1-cf6a8897b989	2026-02-24	Warnings, Adverse reactions	Exact identifier application number: M015
Zinc Oxide and Menthol	ZINC OXIDE, MENTHOL	Akron Formulations India Private Limited	4b84556c-521f-eebd-e063-6394a90a8e1e	2026-02-23	Warnings	Exact identifier application number: M015
Calprotect	MENTHOL, ZINC OXIDE	Reliable 1 Laboratories LLC	09fb2810-0cc1-b2e2-e063-6294a90a4576	2026-02-19	Warnings	Exact identifier application number: M015
Oxify	LIDOCAINE 5%	Weeks & Leo Compnay, INC.	41d9d0b4-33e7-7e05-e063-6394a90a1011	2026-02-17	Warnings	Exact identifier application number: M015
WowDay Hemorrhoid and Fissure Cream	HEMORRHOID AND FISSURE CREAM	WowDay LLC	47ba86ad-240a-e733-e063-6394a90a24e3	2026-02-12	Warnings	Exact identifier application number: M015
Gniby - LIDOCAINE ANORECTAL HEMORRHOIDAL	NUMBING	Putian Licheng District Zhijiancheng Trading Co., Ltd.	4a5f59f1-c11a-e2eb-e063-6394a90a3e27	2026-02-10	Warnings	Exact identifier application number: M015
Numb Master	LIDOCAINE	Clinical Resolution Laboratory, Inc.	0921c824-a8a9-4707-a480-c750192983f5	2026-02-09	Warnings	Exact identifier application number: M015
Signature Care Hemorrhoidal	MINERAL OIL, PETROLATUM, AND PHENYLEPHRINE HCI	Better Living Brands, LLC	3c8b43f3-6e1e-499e-ba71-ffdf836f6743	2026-02-05	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
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