HUMCO GENTIAN VIOLET 1%- gentian violet 1% liquid

Χώρα: Ηνωμένες Πολιτείες

Γλώσσα: Αγγλικά

Πηγή: NLM (National Library of Medicine)

Δραστική ουσία:

GENTIAN VIOLET (UNII: J4Z741D6O5) (GENTIAN VIOLET CATION - UNII:3GVJ31T6YY)

Διαθέσιμο από:

Humco Holding Group, Inc.

INN (Διεθνής Όνομα):

GENTIAN VIOLET

Σύνθεση:

GENTIAN VIOLET 10 mg in 1 mL

Οδός χορήγησης:

TOPICAL

Τρόπος διάθεσης:

OTC DRUG

Θεραπευτικές ενδείξεις:

Antiseptic For external treatment of abrasions, minor cuts, surface injuries, ad superficial infections of the skin. redness, irritation, swelling or pain persists or increases or if infection ocurs.

Καθεστώς αδειοδότησης:

OTC monograph not final

Αρχείο Π.Χ.Π.

HUMCO GENTIAN VIOLET 1%- GENTIAN VIOLET 1% LIQUID
HUMCO HOLDING GROUP, INC.
----------
HUMCO GENTIAN VIOLET 1%
Drug facts
ACTIVE INGREDIENT
Gentian Violet 1%
PURPOSE
Antiseptic
USES
For external treatment of abrasions, minor cuts, surface injuries, ad
superficial
infections of the skin.
WARNINGS
For external use only.
Do not apply to an ulcerative lesion as this may cause tatooing of the
skin. Do not use in
the eyes.
ASK A DOCTOR BEFORE USE IF
redness, irritation, swelling or pain persists or increases or if
infection ocurs.
KEEP OUT OF REACH OF CHILDREN.
In case of accidental ingestion, seek professional assistance or
contact a Poison Control
Center right away.
DIRECTIONS
Clean the affected area and apply directly to the wound or use cotton
applicator once or
twice daily. Do not bandage.
OTHER INFORMATION
will stain skin or clothing.
INACTIVE INGREDIENTS
Ethyl alcohol and purified water.
QUESTIONS OR COMMENTS?
1-800-662-3435
PRINCIPAL DISPLAY PANEL
Label
HUMCO GENTIAN VIOLET 1%
gentian violet 1% liquid
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:0395-1003
ROUTE OF ADMINISTRATION
TOPICAL
Humco Holding Group, Inc.
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF
STRENGTH
STRENGTH
GENTIAN VIOLET (UNII: J4Z741D6O5) (GENTIAN VIOLET CATION -
UNII:3GVJ31T6YY)
GENTIAN VIOLET
10 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)
PACKAGING
# ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:0395-
1003-92
59 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
M003
01/01/2008
LABELER -
Humco Holding Group, Inc. (825672884)
REGISTRANT -
Pharma Nobis, LLC (118564114)
ESTABLISHMENT
NAME
ADDRESS
ID/FEI
BUSINESS OPERATIONS
Pharma Nobis,
LLC
118564114
manufacture(0395-1003) , analysis(0395-1003) , pack(0395-1003) ,
label(0395-1003)
Revised: 12/2023