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 8 of 23 · 441 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hemorrhoid, Fissure, ProctalgiaSuppositories	CARBON, MIRABILITE, PEPPERMINT OIL, BORNEOL	WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.	1d40d16a-ee52-463a-e063-6394a90a6077	2026-01-14	Warnings	Exact identifier application number: M015
Hemorrhoid, Fissure, Proctalgia Relief Wash	CARBON, PANTHENOL, SODIUM HYALURONATE	WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.	1e20de39-45b0-54ec-e063-6294a90a04ed	2026-01-14	Warnings	Exact identifier application number: M015
Hemorrhoid, Fissure, Proctalgia Ointments	CARBON, MIRABILITE, PEPPERMINT OIL, BORNEOL, GLYCERIN	WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.	1efe43d5-a29b-5cb2-e063-6394a90aca66	2026-01-14	Warnings	Exact identifier application number: M015
LONAZEM	MENTHOL,PETROLATUM	PEER PHARM LTD.	91f7a741-4178-4639-9cd5-746a4b9a21bf	2026-01-12	Warnings	Exact identifier application number: M015
Hemorrhoidal Hygiene pads	WITCH HAZEL	Akron Pharma Inc.	936a0cca-5049-4ddf-9581-75c2da6d9cfa	2026-01-12	Warnings	Exact identifier application number: M015
Signature numbing cream	5% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	4805ba4e-45d3-bf0a-e063-6294a90a6eef	2026-01-10	Warnings	Exact identifier application number: M015
THE SOLUTION 2.0	LIDOCAINE	SCALP TECH INC	0fa423b6-cc0f-b569-e063-6294a90a239e	2026-01-09	Warnings	Exact identifier application number: M015
BLACK LABEL B NUMB	LIDOCAINE HYDROCHLORIDE	SCALP TECH INC	11fcf401-0891-04bc-e063-6294a90a8ad5	2026-01-09	Warnings	Exact identifier application number: M015
GOLD LABEL B NUMB	LIDOCAINE HYDROCHLORIDE, EPINEPHRINE HYDROCHLORIDE	SCALP TECH INC	1211590a-13b5-2e75-e063-6394a90a0f86	2026-01-09	Warnings	Exact identifier application number: M015
0.25 % PHENYLEPHRINE HCl HEMORRHOIDAL	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE	Universal Distribution Center LLC	90844919-f16a-4390-9dca-b0405b501445	2026-01-08	Warnings	Exact identifier application number: M015
Signature numbing cream	5% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	47dda425-86d8-441e-e063-6294a90a0f9a	2026-01-08	Warnings	Exact identifier application number: M015
AER Traveler Towelette	AER TRAVELER	Birchwood Laboratories LLC	26556b9b-1c3a-6cf5-e063-6394a90ab26c	2026-01-08	Warnings	Exact identifier application number: M015
Preparation H Rapid Relief	GLYCERIN, LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE	Haleon US Holdings LLC	49a93cfc-4ccd-4ef3-928f-901b9926f794	2026-01-08	Warnings	Exact identifier application number: M015
PREPARATION H FOR WOMEN	WITCH HAZEL	Haleon US Holdings LLC	a9099cf4-4e2e-4cf1-a52f-48f8e174cb15	2026-01-08	Warnings	Exact identifier application number: M015
LIPOCAINE 5	LIDOCAINE 5%	ESBA LABORATORIES INC.	849d6e28-a6b8-7f49-e053-2a91aa0a497d	2026-01-08	Warnings	Exact identifier application number: M015
TOPICAINE 5	LIDOCAINE 5%	ESBA LABORATORIES INC.	15d33ff7-34ed-253d-e054-00144ff88e88	2026-01-08	Warnings	Exact identifier application number: M015
Dr Wellskin Numbing Cream	5% LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	47ebedc5-caf1-a774-e063-6394a90ae14d	2026-01-08	Warnings	Exact identifier application number: M015
Dr. Care Numbing Cream	LIDOCAINE	Shengnan (Guangzhou) Cosmetics Co., LTD	47c94198-7718-bbc2-e063-6294a90a48f1	2026-01-07	Warnings	Exact identifier application number: M015
Healthwise Anorectal Pain Relief	LIDOCAINE 5%	Veridian Healthcare	19c24e1b-a31b-478b-a48b-c39bb4753ca7	2026-01-06	Warnings	Exact identifier application number: M015
Good Sense Hemorrhoidal Maximum Strength Pain Relief	GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM	L. Perrigo Company	1d6142b6-3746-46f1-99ec-4b19d26f056e	2026-01-06	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