Witch Hazel

Product NDC: 41520-822
11-digit product format: 415200822
Labeler code: 41520
Product ID: 41520-822_55648c77-8f5a-b589-e063-6394a90af031
Type: HUMAN OTC DRUG
Nonproprietary name: Witch Hazel
Dosage form: LIQUID
Route: TOPICAL
Labeler: ADUSA Distribution, LLC
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-03-24
Substance: WITCH HAZEL
Active strength: 860 mg/mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

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
c50d0496-6f09-43c2-9383-3250885968c9	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41520-822-43	Witch Hazel	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
WITCH HAZEL	ACTIVE INGREDIENT	101I4J0U34	WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC]	1
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41520-822	WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC]	13	Current NDC, Legacy NDC, 1 package rows	20240907_c50d0496-6f09-43c2-9383-3250885968c9.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 15 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BODY ACTION PRODUCTS Anal Glide Extra	BENZOCAINE	PRODUCT MAX GROUP INC	282ac8d3-2caf-42de-b347-450e9c7a9e50	2025-04-03	Warnings	Exact identifier application number: M015
Numb 520	LIDOCAINE	Clinical Resolution Laboratory, Inc.	984c4bee-0d44-4e0f-a057-0d54400c4cac	2025-04-02	Warnings	Exact identifier application number: M015
hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Bionpharma Inc.	1790da99-2a22-e2a2-e063-6394a90ac36f	2025-03-31	Warnings	Exact identifier application number: M015
HemAway	LIDOCAINE	Melaleuca, Inc.	cf842adf-fcd7-2c8c-e053-2995a90adea6	2025-03-27	Warnings	Exact identifier application number: M015
Numb and Number Anorectal Cream	LIDOCAINE	Dermtech Labs, Inc	31420635-5021-173d-e063-6294a90a407a	2025-03-26	Warnings	Exact identifier application number: M015
Leader Maximum Strength Hemorrhoidal Relief	LIDOCAINE	Cardinal Health,Inc.	65c780b0-7f47-4ae9-a847-c22deaaa2888	2025-03-21	Warnings	Exact identifier application number: M015
Curist Hemorrhoid Fissure Relief	LIDOCAINE	Little Pharma, Inc	2fb02b00-acdb-5184-e063-6294a90ae1c8	2025-03-06	Warnings	Exact identifier application number: M015
Thera Plus Hemorrhoidal	GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE	FOURSTAR GROUP USA, INC.	87143a7a-7b2d-4b67-afda-2355697e7300	2025-03-04	Warnings	Exact identifier application number: M015
Numbskin Maximum Strength Pain Reliever	LIDOCAINE	Shinpharma Inc	2f288bde-99fd-42f8-e063-6394a90a0f05	2025-02-27	Warnings	Exact identifier application number: M015
PREPARATION H TOTABLES IRRITATION RELIEF WIPES	WITCH HAZEL	Haleon US Holdings LLC	1953ec64-20ce-488b-8f14-44e15cc9e720	2025-02-21	Warnings	Exact identifier application number: M015
LBRI STOP THE PAIN Super Aloe Pain Relief Cream	MENTHOL, METHYL SALICYLATE	L'BRI HEALTH AND BEAUTY INC	62e18a37-c0db-4b1e-a6a1-35684cc00e08	2025-01-28	Warnings	Exact identifier application number: M015
Hemorrhoidal	PAIN RELIEF	NeilMed Pharmaceuticals Inc.	038a2cf5-1b72-227b-e063-6394a90a84ad	2025-01-24	Warnings	Exact identifier application number: M015
lidocaine	LIDOCAINE	Nivagen Pharmaceuticals, Inc.	32964ec3-1880-477b-9f71-2222c39106aa	2025-01-23	Warnings	Exact identifier application number: M015
Hemorrhoidal cocoa butter	HEMORRHOIDAL	NeilMed Pharmaceuticals Inc.	03b159b0-b960-b38d-e063-6394a90a9462	2025-01-17	Warnings	Exact identifier application number: M015
Gentle Laxative Bisacodyl	GENTLE LAXATIVE BISACODYL	NeilMed Pharmaceuticals Inc	03b3733a-4d78-149f-e063-6294a90a6518	2025-01-17	Warnings	Exact identifier application number: M015
Glycerin Laxative	GLYCERIN BASED GENTLE AND EFFECTIVE LAXATIVE ADULT CONSTIPATION RELIEF	NeilMed Pharmaceuticals Inc.	03b4be69-6488-76be-e063-6394a90a7edf	2025-01-17	Warnings	Exact identifier application number: M015
Pre-moistened Medicated Wipes, Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent, Walgreens Pre-moistened Medicated Wipes, Walgreens Pre-moistened Medicated Wipes Witch Hazel 50%/Hemorrhoidal Astringent	WITCH HAZEL	Walgreens Company	209a111b-d169-cb5d-e063-6394a90a33ca	2025-01-15	Warnings	Exact identifier application number: M015
Pre-moistened Medicated Pads, Pre-moistened Medicated Pads Hemorrhoidal Pads with Witch Hazel, Walgreens Pre-moistened Medicated Pads, Walgreens Pre-moistened Medicated Pads Hemorrhoidal Pads with Witch Hazel	WITCH HAZEL	Walgreens Company	1e2dcec1-a1fe-71d2-e063-6394a90a9908	2025-01-15	Warnings	Exact identifier application number: M015
AER Pre-moistened Witch Hazel Pad	WITCH HAZEL	Birchwood Laboratories LLC	1cca622f-0a6b-4f35-9355-34c249ee705e	2025-01-14	Warnings	Exact identifier application number: M015
B-SURE Traveler Towelette	B-SURE TRAVELER	Birchwood Laboratories LLC	e1a5da94-6a1a-497b-a737-1c1541bf0404	2025-01-14	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	c50d0496-6f09-43c2-9383-3250885968c9	16
200295	witch hazel 860 MG/ML Topical Solution	SCD	c50d0496-6f09-43c2-9383-3250885968c9	16
200295	witch hazel 86 % Topical Solution	SY	c50d0496-6f09-43c2-9383-3250885968c9	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
41520-822-43	41520082243	473 mL in 1 BOTTLE, PLASTIC (41520-822-43)	473 ml	2015-03-24	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Care One 822.002/822AA Witch Hazel	ADUSA Distribution, LLC \| Nice-Pak Products, LLC	2026-06-29	HUMAN OTC DRUG LABEL	17