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 21 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mayinglong Hemorrhoidal	PETROLATUM, ZINC OXIDE	Mayinglong Pharmaceutical Group Co., Ltd.	b14192ea-1bf7-da6a-e053-2a95a90a5b5e	2023-12-08	Warnings	Exact identifier application number: M015
Hemorrhoidal cooling gel	PHENYLEPHRINE HCL, WITCH HAZEL	WALGREENS	03bbe258-e00d-13cc-e063-6394a90ae345	2023-12-05	Warnings	Exact identifier application number: M015
Hemorrhoidal Pain Relief	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	WALGREENS	03bc5c1a-d493-5082-e063-6394a90ae87b	2023-12-05	Warnings	Exact identifier application number: M015
Bloop Hemorrhoid Relief Topical	GLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCL	Three Nations Corp	0b6419e3-f1c7-bdfe-e063-6294a90a5d92	2023-11-30	Warnings	Exact identifier application number: M015
Bloop Fissure Healing Anorectal Topical	LIDOCAINE	Three Nations Corp	0b645092-ebc4-e4bb-e063-6294a90ad4cf	2023-11-30	Warnings	Exact identifier application number: M015
SIMPLY VITAL HEMORRHOID and ANORECTAL RELIEF	LIDOCAINE	ALPHA PLANTS INC	79fa4b89-382f-45fa-a792-90a9fe5bf573	2023-11-11	Warnings	Exact identifier application number: M015
BODY ACTION PRODUCTS Prolong Lubricating	BENZOCAINE	PRODUCT MAX GROUP INC	3bef5915-1c98-4011-baa9-ad0bbef200c2	2023-11-10	Warnings	Exact identifier application number: M015
BODY ACTION PRODUCTS Butt Eze Benzocaine	BENZOCAINE	PRODUCT MAX GROUP INC	ba75b129-7939-4373-91f5-1772976e6d61	2023-11-10	Warnings	Exact identifier application number: M015
Uber Numb Topical Anesthetic	LIDOCAINE HYDROCHLORIDE	UberScientific, LLC	441c802f-a363-1530-e054-00144ff88e88	2023-11-10	Warnings	Exact identifier application number: M015
Uber Numb Topical Anesthetic	LIDOCAINE HYDROCHLORIDE	UberScientific, LLC	4939a547-c94b-3350-e054-00144ff88e88	2023-11-10	Warnings	Exact identifier application number: M015
DR REAL NUMB Topical Anorectal	LIDOCAINE	FUZZYLULU LLC	378d8edc-2120-416d-854c-8881c2950efe	2023-11-09	Warnings	Exact identifier application number: M015
The Pharma C Company Medicated Foam with Witch Hazel	WITCH HAZEL	Kleen Test Products Corporation	1a1fbe83-be45-4654-a7bb-e934e1ccd0c6	2023-11-09	Warnings	Exact identifier application number: M015
The Pharma-C Company Medicated Hemorrhoidal Pads	WITCH HAZEL	Kleen Test Products Corporation	357703ab-4e7a-41f6-9ecf-aa98acc2d92e	2023-11-09	Warnings	Exact identifier application number: M015
DOCTORS TOUCH Erase The Pain Lidocaine	LIDOCAINE HYDROCHLORIDE	DOCTOR'S CHOICE MEDICAL, LLC	3dc9947b-8196-4a38-97b4-c2340ee77e0f	2023-11-06	Warnings	Exact identifier application number: M015
SCALAR Pain Relief Cream	MENTHOL	Miracle Balance, LLC	52a13cfe-3f46-45f8-a5af-ce07ea5758e3	2023-11-06	Warnings	Exact identifier application number: M015
SIMPLE PROMISE Simple H Hemorrhoid Relief Cream	PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE	SIMPLE PROMISE PTE LTD	f6622caa-3b31-9b07-e053-2a95a90a8a51	2023-11-06	Warnings	Exact identifier application number: M015
WAXUP Numbing	LIDOCAINE HYDROCHLORIDE	CONSTRUSOLUTION, LLC	4f1645ab-1b19-4d69-99c3-9ea275b01a87	2023-11-06	Warnings	Exact identifier application number: M015
SECONDARY NUMB Lidocaine Phenylephrine Gel	LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE	LALANI Rx Consulting, Inc.	0f13f7b5-e3b1-451e-a6d6-e7e15bd04443	2023-11-06	Warnings	Exact identifier application number: M015
Brazzers Anal Desensitizing	LIDOCAINE	Metro Media Ent	ceacd80c-0dd6-4e21-97da-56da877b1c90	2023-11-06	Warnings	Exact identifier application number: M015
NUMB PLUS Maximum Strength Anorectal	LIDOCAINE	SEENEXT VENTURE LTD	a7c37b2a-b647-43d7-b43b-87bbece35430	2023-11-05	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