Witch Hazel

Product NDC: 41250-822
11-digit product format: 412500822
Labeler code: 41250
Product ID: 41250-822_4b34762c-db2f-f8ba-e063-6394a90a273d
Type: HUMAN OTC DRUG
Nonproprietary name: WITCH HAZEL
Dosage form: LIQUID
Route: TOPICAL
Labeler: Meijer, Inc.
Application: M016
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1996-03-15
Substance: WITCH HAZEL
Active strength: 86 kg/100L
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	41250-822	41250-822-99	D	Discontinued by firm		2026-10-15

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 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	41250-822	41250-822-99	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	41250-822	41250-822-99	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

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	86 kg/100L

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
13e4aece-5b91-4f89-a912-540bf170a8d1	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41250-822-43	Witch Hazel	0.473 L in 1 BOTTLE, PLASTIC	LIQUID	0.473		20
41250-822-99	Witch Hazel	0.236 L in 1 BOTTLE, PUMP	LIQUID	0.236		20

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
WITCH HAZEL	ACTIVE INGREDIENT	101I4J0U34	WITCH HAZEL LIQUID [MEIJER DISTRIBUTION, INC]	1
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	WITCH HAZEL LIQUID [MEIJER DISTRIBUTION, INC]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	WITCH HAZEL LIQUID [MEIJER DISTRIBUTION, INC]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41250-822	WITCH HAZEL LIQUID [MEIJER DISTRIBUTION, INC]	18	Current NDC, Legacy NDC, 2 package rows	20241114_13e4aece-5b91-4f89-a912-540bf170a8d1.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 13 of 68 · 1,357 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Colloidal oatmeal	COLLOIDAL OATMEAL	CVS Pharmacy, Inc.	4a43b1a2-2156-e490-e063-6294a90a6f84	2026-04-07	Warnings, Adverse reactions	Exact identifier application number: M016
Calamine	CALAMINE 8%, ZINC OXIDE 8%	Farmacias De Similares TX LLC	4ecd0add-11c9-cf3b-e063-6394a90adff6	2026-04-06	Warnings	Exact identifier application number: M016
Petroleum	WHITE PETROLATUM	CVS Pharmacy, Inc.	4dc08832-e610-4e62-a6af-cadaa339e39e	2026-04-06	Warnings, Adverse reactions	Exact identifier application number: M016
Witch Hazel	WITCH HAZEL SPRAY	CVS Pharmacy	53db78a8-eb2d-431b-84c1-73e99bb9d3d1	2026-04-06	Warnings	Exact identifier application number: M016
Petroleum	WHITE PETROLATUM	Amazon.com Services LLC	616ef87d-1518-46aa-8e12-9a1b678d4980	2026-04-06	Warnings, Adverse reactions	Exact identifier application number: M016
Stabilizing Repair Serum	OATMEAL	Dermalogica, LLC.	86b7b230-5424-46d3-8058-656f5172fc70	2026-04-02	Warnings	Exact identifier application number: M016
calamine	CALAMINE AND ZINC OXIDE	STRATEGIC SOURCING SERVICES	4e6a7bdf-4ef1-65e2-e063-6394a90ae124	2026-04-01	Warnings	Exact identifier application number: M016
Aveeno Eczema Therapy Rescue Relief Treatment Gel Cream	COLLOIDAL OATMEAL	Kenvue Brands LLC	4e4e1797-26e6-a67b-e063-6294a90af438	2026-03-31	Warnings	Exact identifier application number: M016
Target Advanced Scar Gel	ADVANCED SCAR GEL	Target Corporation	86c215fe-aad4-45d1-bdb7-cde00a115c5c	2026-03-31	Warnings	Exact identifier application number: M016
Zinc oxide, Dimethicone	ZINC OXIDE, DIMETHICONE	Walmart Inc.	4cbf9492-33cd-e6d4-e063-6294a90ab001	2026-03-31	Warnings, Adverse reactions	Exact identifier application number: M016
Critic-Aid Clear	PETROLATUM	Coloplast Corp	a92c18f7-52b2-43e4-bae3-2bab9de22671	2026-03-31	Warnings	Exact identifier application number: M016
3M Cavilon Durable Barrier	DIMETHICONE	Solventum US LLC	f3f8be33-4ad2-4f5f-ac94-ddfbe0280b83	2026-03-31	Warnings	Exact identifier application number: M016
XIMONTH Foot Sanitizer	GLYCERIN	Shantou Ximonth Biotechnology Co., Ltd.	4e38d24d-3745-c121-e063-6394a90abbb5	2026-03-30	Warnings	Exact identifier application number: M016
Dynashield	ZINC OXIDE	Dynarex Corporation	59fd865c-b81d-43ad-8fa0-c37ca0557769	2026-03-30	Warnings	Exact identifier application number: M016
First Aid Beauty FAB Ultra Repair Intense Hydration Skin Protectant	COLLOIDAL OATMEAL	Port Jervis Laboratories, Inc	4e43b65c-d5bb-f228-e063-6294a90ad08d	2026-03-30	Warnings	Exact identifier application number: M016
ChapStick Classic Original	SKIN PROTECTANT LIP BALM	Suave Brands Co., LLC	4275956d-275a-4e31-e063-6394a90a78d3	2026-03-30	Warnings	Exact identifier application number: M016
ChapStick Classic Cherry	SKIN PROTECTANT LIP BALM	Suave Brands Co., LLC	42762471-e5cd-505e-e063-6294a90afb7d	2026-03-30	Warnings	Exact identifier application number: M016
ChapStick Classic Variety Cherry-Strawberry-Spearmint	SKIN PROTECTANT LIP BALM	Suave Brands Co., LLC	450e46d2-de86-e5fa-e063-6294a90ac6ff	2026-03-30	Warnings	Exact identifier application number: M016
ChapStick Classic Original	SKIN PROTECTANT LIP BALM	Suave Brands Co., LLC	4512220a-9fc2-8816-e063-6394a90a9d15	2026-03-30	Warnings	Exact identifier application number: M016
ChapStick Classic Original Military	SKIN PROTECTANT LIP BALM	Suave Brands Co., LLC	45136b7e-136b-0283-e063-6394a90a599a	2026-03-30	Warnings	Exact identifier application number: M016

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	13e4aece-5b91-4f89-a912-540bf170a8d1	20
200295	witch hazel 860 MG/ML Topical Solution	SCD	13e4aece-5b91-4f89-a912-540bf170a8d1	20
200295	witch hazel 86 % Topical Solution	SY	13e4aece-5b91-4f89-a912-540bf170a8d1	20

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
41250-822-43	41250082243	.473 L in 1 BOTTLE, PLASTIC (41250-822-43)	1996-03-15	0000-00-00	No	No	Current
41250-822-99	41250082299	.236 L in 1 BOTTLE, PUMP (41250-822-99)	1996-03-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meijer 822.001/822AA Witch Hazel	Meijer, Inc. \| Nice-Pak Products, LLC	2026-02-19	HUMAN OTC DRUG LABEL	20