WITCH HAZEL liquid

Država: Sjedinjene Američke Države

Jezik: engleski

Izvor: NLM (National Library of Medicine)

Aktivni sastojci:

WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)

Dostupno od:

Hydrox Laboratories

INN (International ime):

Witch Hazel

Sastav:

Witch Hazel 86 mg in 100 mL

Administracija rute:

TOPICAL

Tip recepta:

OTC DRUG

Terapijske indikacije:

Astringent For relief of minor skin irritations due to insect bites, minor cuts, minor scrapes. Stop use and ask a doctor if Condition worsens or symptoms persist for more than 7 days.

Status autorizacije:

OTC monograph final

Svojstava lijeka

WITCH HAZEL- WITCH HAZEL LIQUID
HYDROX LABORATORIES
----------
WITCH HAZEL
_DRUG FACTS_
ACTIVE INGREDIENT
Witch Hazel 86%
PURPOSE
Astringent
USES
For relief of minor skin irritations due to insect bites, minor cuts,
minor scrapes.
WARNINGS
FOR EXTERNAL USE ONLY.
KEEP OUT OF REACH OF CHILDREN
If swallowed, get medical help or contact a Poison Control Center
right away.
DIRECTIONS
Apply to the affected area as often as necessary. When using this
product, avoid
contact with the eyes.
STOP USE AND ASK A DOCTOR IFCondition worsens or symptoms persist for
more than
7 days.
INACTIVE INGREDIENT
Alcohol 14% by volume
DIST. BY:
HYDROX LABORATORIES
825-B TOLLGATE RD.• ELGIN, IL 60123
PRINCIPAL DISPLAY PANEL - 473 ML BOTTLE LABEL
_PERSONAL CARE_
_FRESHMOMENT_
_WITCH HAZEL_
_NATURAL ASTRINGENT _
_CLEANS AND REFRESHES SKIN _
_NO ARTIFICIAL FRAGRANCE _
_OR DYES_
MADE IN USA
16 FL. OZ. (473ML)
WITCH HAZEL
witch hazel liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:10565-040
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)
WITCH HAZEL
86 g in 100 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
Hydrox Laboratories
ALCOHOL (UNII: 3K9958V90M)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:10565-
040-16
473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a
Combination Product
11/13/2017
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
505G(a)(3)
12/21/2011
LABELER -
Hydrox Laboratories (025164302)
REGISTRANT -
Hydrox Laboratories (025164302)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Hydrox Laboratories
025164302
manufacture(10565-040) , label(10565-040) , pack(10565-040)
Revised: 10/2023