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NDC 10733-0801-08 Witch Hazel 86 g/100mL Details

Witch Hazel 86 g/100mL

Witch Hazel is a TOPICAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Medical Products Laboratories, Inc.. The primary component is WITCH HAZEL.

Product Information

NDC	10733-0801
Product ID	10733-801_bb8db612-ee0c-0a3a-e053-2995a90a79cc
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Witch Hazel
Proprietary Name Suffix	n/a
Non-Proprietary Name	Witch Hazel
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	TOPICAL
Active Ingredient Strength	86
Active Ingredient Units	g/100mL
Substance Name	WITCH HAZEL
Labeler Name	Medical Products Laboratories, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part346
Listing Certified Through	2024-12-31

Package

Package Images

NDC 10733-0801-08 (10733080108)

Pricing Information	N/A
NDC Package Code	10733-801-08
Billing NDC	10733080108
Package	236 mL in 1 BOTTLE, DISPENSING (10733-801-08)
Marketing Start Date	2021-01-29
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL b815792f-2f8f-7ac8-e053-2995a90ade18 Details

Warnings

For external use only

When using this product

avoid contact with the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

condition worsens or symptoms last for more than 7 days

Keep out of reach of children.

If swallowed, get medical help or contact a Posion Control Center right away.

MANUFACTURED BY:

MEDICAL PRODUCTS LABORATORIES, INC.

9990 GLOBAL ROAD, PHILADELPHIA 19115

mplusa.com

Questions or comments? Call 1-800-523-0191

Witch Hazel For Face & Body

ASTRINGENT

Relief of minor skin irritations due to:

Insect bites
Minor cuts & scrapes

Active ingredient

Witch hazel 86%

Purpose

Astringent

Inactive ingredient:

alcohol 14% by volume

Use

for relief of minor skin irritations due to:

• insect bites • minor cuts • minor scrapes

Directions

apply as often as needed

10733-801-08

10733-801-16

INGREDIENTS AND APPEARANCE

WITCH HAZEL

witch hazel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10733-801
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	86 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:10733-801-08	236 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/29/2021
2	NDC:10733-801-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/29/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part346	01/29/2021

Labeler - Medical Products Laboratories, Inc. (002290302)

Registrant - Medical Products Laboratories, Inc. (002290302)

Name	Address	ID/FEI	Business Operations
Establishment
Medical Products Laboratories, Inc.		002290302	pack(10733-801) , manufacture(10733-801) , analysis(10733-801)

Revised: 2/2021

Document Id: bb8db612-ee0c-0a3a-e053-2995a90a79cc

Set id: b815792f-2f8f-7ac8-e053-2995a90ade18

Version: 2

Effective Time: 20210217