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 7 of 23 · 441 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0.25 % PHENYLEPHRINE HCl HEMORRHOIDAL	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE	Nantong Health & Beyond Hygienic Products Inc.	1cada0ae-3f0f-441c-a633-faa0a3009d2b	2026-02-05	Warnings	Exact identifier application number: M015
Numbing Cream	LIDOCAINE	Sainite Trading Shenzhen Co., Ltd.	49fcbe81-34b6-5906-e063-6294a90aa65b	2026-02-04	Warnings	Exact identifier application number: M015
Perineal Cooling Pad Liners	FRIDA MOM PERINEAL COOLING PAD LINERS	Fridababy, LLC	e9d33d92-34ee-b639-e053-2a95a90a9f36	2026-02-04	Warnings	Exact identifier application number: M015
Hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Sportpharm LLC	88e3624d-b8bb-4e65-9250-4c51d2bbed16	2026-02-03	Warnings	Exact identifier application number: M015
careone hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	American Sales Company	46794d2e-8fe6-490d-9cfa-ba9b6c209ad6	2026-01-29	Warnings	Exact identifier application number: M015
LUBRICAINE 5	LIDOCAINE 5%	ESBA LABORATORIES INC.	9d98afbf-11ce-745b-e053-2a95a90abc14	2026-01-28	Warnings	Exact identifier application number: M015
foster and thrive hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Strategic Sourcing Services LLC	9da843f2-e88c-432e-b091-a6acf81d856b	2026-01-22	Warnings	Exact identifier application number: M015
hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	HyVee Inc	bf1beca0-cc9b-4100-9db7-77f2d1e5497c	2026-01-21	Warnings	Exact identifier application number: M015
GRANULOTION Hemorrhoidal	MENTHOL, ZINC OXIDE	GL Health, Inc.	1a32741c-5e4a-40e5-b15a-8233c5bdb92b	2026-01-19	Warnings	Exact identifier application number: M015
Hydroseptine	ZINC OXIDE, MENTHOL	AKRON PHARMA INC	5359d92e-641e-4076-9d91-18daee58a30e	2026-01-19	Warnings	Exact identifier application number: M015
Hemorrhoidal Cream	HEMORRHOIDAL CREAM	Walgreens	1ac2b2ae-c090-483b-ad2c-1374552add4a	2026-01-15	Warnings	Exact identifier application number: M015
Walgreens	HEMORRHOIDAL PAIN RELIEF	Walgreens	b0b1ce47-9fa4-4505-8f38-39a0d500e9f6	2026-01-15	Warnings	Exact identifier application number: M015
Hemorrhoidal Cream	HEMORRHOIDAL CREAM	Walgreens	4276ddad-2363-462a-bb97-574f946ec3f0	2026-01-15	Warnings	Exact identifier application number: M015
Walgreens	HEMORRHOIDAL COOLING GEL	Walgreens	1277d2e8-2a5e-23f5-e063-6294a90a69b0	2026-01-15	Warnings	Exact identifier application number: M015
Hemorrhoid and Fissure	GLYCERIN 6%,LIDOCAINE 4%,ECTOIN 0.12%	FlexiGo Inc	48697377-61c0-1b0a-e063-6294a90a3293	2026-01-15	Warnings	Exact identifier application number: M015
MEDPURA Vitamin A and D Vitamin A and D	MEDPURA VITAMIN A AND D	Akron Pharma Inc.	38cc2317-691b-4657-af05-c67623eba760	2026-01-14	Warnings	Exact identifier application number: M015
Walgreens Hemorrhoidal	HEMORRHOIDAL RECTAL SUPPOSITORIES	Walgreens	2dd710ac-ab04-4a24-826f-b5a44d058168	2026-01-14	Warnings	Exact identifier application number: M015
Walgreens Hemorrhoidal	HEMORRHOIDAL RECTAL SUPPOSITORIES	Walgreens	ca98dea5-767d-49a8-887b-d96cad487fc4	2026-01-14	Warnings	Exact identifier application number: M015
Walgreens Moisture Barrier	MENTHOL, AND ZINC OXIDE	Walgreen Company	a6db6f13-4e02-47dc-aef6-a804506c3d8b	2026-01-14	Warnings	Exact identifier application number: M015
GNP Hemorrhoidal Maximum Strength	HEMORRHOIDAL	Amerisourcebergen Drug Corporation	24103355-cd72-55b0-e063-6394a90a90ec	2026-01-14	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