Witch Hazel

Product NDC: 59779-045
11-digit product format: 597790045
Labeler code: 59779
Product ID: 59779-045_49ed94e0-a9d0-ca73-e063-6394a90a8a51
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		2026-08-17

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…`

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 1 of 22 · 434 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gembooxt Topical Numbing Cream	LIDOCAINE	Guangdong Quadrant Ecological Technology Co., Ltd.	49951a3e-3b62-3d66-e063-6294a90a9360	2026-08-12	Warnings	Exact identifier application number: M015
NumbMD Lidocaine Cream Anorectal(hemorrhoidal)	LIDOCAINE 5%	EveryMarket Inc	52379055-d017-4d98-e063-6294a90a196c	2026-08-12	Warnings	Exact identifier application number: M015
Nupharmisto NumbMD Lidocaine Cream	LIDOCAINE 5%	EveryMarket Inc	52369a41-820d-cd7a-e063-6394a90ac6d1	2026-08-12	Warnings	Exact identifier application number: M015
Nupharmisto NumbMD Lidocaine Cream	LIDOCAINE 5%	EveryMarket Inc	51d370b4-1c34-d203-e063-6394a90a80b1	2026-08-12	Warnings	Exact identifier application number: M015
Nupharmisto NumbMD 5% Lidocaine cream	LIDOCAINE 5%	EveryMarket Inc	507d0c2c-9517-40f8-e063-6394a90a1996	2026-08-12	Warnings	Exact identifier application number: M015
Nupharmisto NumbMD LIDOCAINE cream anorectal (hemorrhoidal)	LIDOCAINE CREAM ANORECTAL	EveryMarket Inc	483d81a3-7493-3391-e063-6394a90a2e3d	2026-08-12	Warnings	Exact identifier application number: M015
Numbing Cream	LIDOCAINE	100 KARMA INC	35b5ba9d-da1d-55d6-e063-6294a90a5fa8	2026-08-12	Warnings	Exact identifier application number: M015
Treatonic hemorrhoid treatment	5% LIDOCAINE	100 KARMA INC	41442fa7-c511-07ca-e063-6294a90a3992	2026-08-12	Warnings	Exact identifier application number: M015
Lidocaine numbing cream	5% LIDOCAINE	100 KARMA INC	47380721-6633-4a50-e063-6394a90aca94	2026-08-12	Warnings	Exact identifier application number: M015
Treatonic 5% Lidocaine Cream	5% LIDOCAINE CREAM	100 KARMA INC	47dc7630-9a74-1989-e063-6294a90a50bb	2026-08-12	Warnings	Exact identifier application number: M015
Treatonic 5% Lidocaine Cream	5% LIDOCAINE CREAM	100 KARMA INC	49e6b69f-bd6e-b415-e063-6394a90a8e65	2026-08-12	Warnings	Exact identifier application number: M015
THE SOLU TION	LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE HYDROCHLORIDE	SCALP TECH INC	58793581-8826-9a74-e063-6294a90a2465	2026-08-06	Warnings	Exact identifier application number: M015
Lidocaine Numbing Cream	LIDOCAINE	Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.	5457b3d7-e6b6-34a7-e063-6394a90aa240	2026-08-03	Warnings	Exact identifier application number: M015
HEMORRHOIDALCREAMPROCURE	PHENYLEPHRINE HCL, PETROLATUM, MINERAL OIL	TWIN MED, LLC	e9c44756-1c98-41be-e053-2995a90a35b4	2026-08-03	Warnings	Exact identifier application number: M015
Lidocaine Hydrochloride	LIDOCAINE HYDROCHLORIDE	YYBA CORP	582a0001-da1e-909a-e063-6394a90a2b11	2026-08-03	Warnings	Exact identifier application number: M015
up and up	PHENYLEPHRINE HYDROCHLORIDE	Target Corporation	b42775ae-44fe-487e-b9ca-21d9687020a9	2026-07-29	Warnings	Exact identifier application number: M015
Acolye Numbing Cream Anorectal(Hemorrhoidal) Cream	LIDOCAINE	Guangdong Aimu Biological Technology Co., Ltd	578fa642-ff30-e511-e063-6294a90a5987	2026-07-26	Warnings	Exact identifier application number: M015
CVS Topical Anesthetic Hemorrhoidal	DIBUCAINE	CVS PHARMACY, INC	9f3d4fdb-ad82-4ab8-8a9e-252d027068ab	2026-07-25	Warnings	Exact identifier application number: M015
Moisture Barrier	MENTHOL 0.44%, ZINC OXIDE 20.6%	Walgreen Company	258f3392-0f42-21e8-e063-6294a90ae9ad	2026-07-22	Warnings	Exact identifier application number: M015
RectaEase Hemorrhoid Relief Cream	LIDOCAINE	Trifecta Pharmaceuticals USA LLC	c054921a-9f1b-7c75-e053-2995a90a1738	2026-07-20	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