Witch Hazel

Product NDC: 37808-822
11-digit product format: 378080822
Labeler code: 37808
Product ID: 37808-822_560688dc-1e94-094b-e063-6294a90ae436
Type: HUMAN OTC DRUG
Nonproprietary name: Witch Hazel
Dosage form: LIQUID
Route: TOPICAL
Labeler: H E B
Application: M015
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-06-18
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	37808-822	37808-822-45	D	Discontinued by firm		2026-10-15
excluded package	package	37808-822	37808-822-99	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 · 4 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	37808-822-45	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	37808-822-99	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	37808-822-45	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	37808-822-99	`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	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
09b814f4-86b5-4810-bf52-cc88396451c2	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	SPL version
37808-822-43	Witch Hazel	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473	16
37808-822-45	Witch Hazel	946 mL in 1 BOTTLE, PLASTIC	LIQUID	946	16
37808-822-99	Witch Hazel	236 mL in 1 BOTTLE, PUMP	LIQUID	236	16

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
WITCH HAZEL	ACTIVE INGREDIENT	101I4J0U34	WITCH HAZEL LIQUID [H-E-B]	1
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	WITCH HAZEL LIQUID [H-E-B]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	WITCH HAZEL LIQUID [H-E-B]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-822	WITCH HAZEL LIQUID [H-E-B]	14	Current NDC, Legacy NDC, 3 package rows	20240922_09b814f4-86b5-4810-bf52-cc88396451c2.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 10 of 22 · 438 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pranicura 5	GLYCERIN, KAOLIN, CALAMINE, MENTHOL	Pranicura Products LLC	af520a58-3f3c-4d28-a41f-3ed8f74da095	2025-11-04	Warnings	Exact identifier application number: M015
ProCure ClamaPlex	ZINC OXIDE 20.625, MENTHOL 0.44, WHITE PETROLATUM 66.335	Twin Med LLC	3d366857-5178-9032-e063-6294a90a40f3	2025-11-01	Warnings	Exact identifier application number: M015
GNP Hemorrhoidal	MINERAL OIL, PETROLATUM, PHENYLEPHRINE, HCL	Amerisource Bergen	b0f0ef97-9add-717f-e053-2a95a90a0eb0	2025-10-30	Warnings	Exact identifier application number: M015
REMEDY Calazime Skin Protectant	CALAMINE, MENTHOL, WHITE PETROLATUM, ZINC OXIDE	Medline Industries, LP	1295cfcc-5b61-481b-964b-f53ffd0cb58e	2025-10-30	Warnings	Exact identifier application number: M015
Hemorrhoid Anesthetic	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	Universal Distribution Center LLC	186c2d32-e8c5-d13d-e063-6294a90a2b0e	2025-10-30	Warnings	Exact identifier application number: M015
Workvie	LIDOCAINE HCL, MENTHOL	Marketites LLC	aebaffb5-58dd-ebd5-e053-2a95a90a14ed	2025-10-29	Warnings	Exact identifier application number: M015
hemorrhoidal	GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM	Publix Super Markets Inc	354a640c-bc7e-45c8-9df0-8b5b01767f5c	2025-10-29	Warnings	Exact identifier application number: M015
Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	Pharmacy Value Alliance LLC	903b77fc-02bf-73b6-e053-2a95a90ad4cc	2025-10-24	Warnings	Exact identifier application number: M015
Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	CVS Pharmacy	845fc11b-707d-2027-e053-2991aa0a1c8a	2025-10-24	Warnings	Exact identifier application number: M015
Calmol 4	ZINC OXIDE AND COCOA BUTTER	Resical Inc.	5516f800-d3fa-4b90-a3eb-c0bdf3183b9b	2025-10-24	Warnings	Exact identifier application number: M015
Hemorrhoidal	COCOA BUTTER, PHENYLEPHRINE HCL	Amerisourcebergen Drug Corporation	231a850a-bad6-9a30-e063-6394a90a0fdc	2025-10-24	Warnings	Exact identifier application number: M015
Signature Care Hemorrhoidal Cream (with applicator)	PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, GLYCERIN, PETROLATUM	BETTER LIVING BRANDS, LLC	b026a386-5e38-52ed-e053-2a95a90a6b0e	2025-10-24	Warnings	Exact identifier application number: M015
Americaine	BENZOCAINE	Insight Pharmaceuticals LLC	d13c022f-2f91-40b4-bd66-0cfc0e147a5f	2025-10-23	Warnings	Exact identifier application number: M015
Winco Hemorrhoidal	MINERAL OIL, PETROLATUM, AND PHENYLEPHRINE HYDROCHLORIDE	Winco Foods, LLC	04ca3ef1-fc6b-4683-b236-a75afc031fb5	2025-10-23	Warnings	Exact identifier application number: M015
Signature Care Medicated Cooling	WITCH HAZEL	Better Living Brands, LLC	b35dc719-a5a2-4839-870d-25313d3f7c9b	2025-10-22	Warnings	Exact identifier application number: M015
Family Care Hemorrhoidal	MINERAL OIL	United Exchange Corp	04375257-f4f3-48c3-a338-de43298b95eb	2025-10-22	Warnings	Exact identifier application number: M015
Family Wellness Hemorrhoidal	MINERAL OIL, PETROLATUM, AND PHENYLEPHRINE HCL	Family Dollar Services, Inc	fe3293bc-80b5-b60a-e053-6394a90a4ede	2025-10-22	Warnings	Exact identifier application number: M015
Xesso Rear Comfort Glide	LIDOCAINE	PREMIUM NATURAL COSMETICS INC	e9eb262e-a1c1-7d5c-e053-2a95a90a7c9f	2025-10-22	Warnings	Exact identifier application number: M015
Adellina Lidocaine Numbing Cream Anorectal(Hemorrhoidal) Cream	LIDOCAINE	Guangzhou Haishi Biological Technology Co., Ltd.	41a6d309-2722-1738-e063-6294a90a8a70	2025-10-21	Warnings	Exact identifier application number: M015
DERMOSCRIBE ICHYBUM	HYDROCORTISONE, CLIOQUINOL, ZINC OXIDE	DERMOSCRIBE PTY LTD	134a88a1-13e5-4da0-8270-c380b57aaeb7	2025-10-17	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	09b814f4-86b5-4810-bf52-cc88396451c2	16
200295	witch hazel 860 MG/ML Topical Solution	SCD	09b814f4-86b5-4810-bf52-cc88396451c2	16
200295	witch hazel 86 % Topical Solution	SY	09b814f4-86b5-4810-bf52-cc88396451c2	16

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37808-822-43	37808082243	473 mL in 1 BOTTLE, PLASTIC (37808-822-43)	473 ml	2015-06-18	0000-00-00	No	No	Current
37808-822-45	37808082245	946 mL in 1 BOTTLE, PLASTIC (37808-822-45)	946 ml	2015-06-18	0000-00-00	No	No	Current
37808-822-99	37808082299	236 mL in 1 BOTTLE, PUMP (37808-822-99)	236 ml	2015-06-18	0000-00-00	No	No	Current