ZYLOTROL MAXIMUM PAIN PATCH- lidocaine 4%, menthol 1% patch

País: Estats Units

Idioma: anglès

Font: NLM (National Library of Medicine)

Compra'l ara

Descargar Fitxa tècnica (SPC)
20-10-2023

ingredients actius:

LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987), MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)

Disponible des:

Whitestone Products LLC

Vía de administración:

TOPICAL

tipo de receta:

OTC DRUG

indicaciones terapéuticas:

Topical Analgesic - in large quantities, particularly over raw surfaces, or blistered areas. For the temporary relief of pain.

Estat d'Autorització:

OTC monograph not final

Fitxa tècnica

                                ZYLOTROL MAXIMUM PAIN PATCH- LIDOCAINE 4%, MENTHOL 1% PATCH
WHITESTONE PRODUCTS LLC
----------
ZYLOTROL FOR PAIN CONTROL LIDOCAINE 4% AND MENTHOL 1%
Lidocaine 4%
Menthol 1%
Topical Analgesic
FOR EXTERNAL USE ONLYnot intended for ingestion.
in large quantities, particularly over raw surfaces, or blistered
areas.
Avoid contact with eyes.
condition worsens, or if symtoms persist for more than 7 days or clear
up and occur
again within a few days.
If swallowed, get medical help, or contact a Poison Control Central
right away.
ask a health professional before use.
DIRECTIONS
Adults and children 2 years of age and older: Apply to affected area
not more than 3
to 4 times a daily.
Children under 2 years of age: consult a doctor.
Store at 20-25oC (68-77oF) and protect from moisture.
polyacrylamide, vinol, sodium polyacrylate; acrylate polymerization;
purified water.
QUESTIONS?
(310) 320-0100
USES
For the temporary relief of pain.
ZYLOTROL MAXIMUM PAIN PATCH
lidocaine 4%, menthol 1% patch
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:81902-101
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH STRENGTH
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)
LIDOCAINE
4 g
in 100 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED
FORM - UNII:L7T10EIP3A)
MENTHOL, UNSPECIFIED
FORM
1 g
in 100 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
Whitestone Products LLC
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
ETHENYL (UNII: PQ2K3G3591)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:81902-101-
15
15 in 1 BOX
07/30/2021
1
4 g in 1 PATCH; Type 0: Not a Combination
Product
MARKETING INFORMATION
MARKETING
CATEGORY
APPLICATION NUMBER OR MONOGRAPH
CITATION
MARKETING START
DATE
MARKETING END
DATE
OTC Monograph Drug
505G(a)(3)
07/30/2021
LABELER -
Whitestone Products LLC (118064415)
Revise
                                
                                Llegiu el document complet
                                
                            

Cerqueu alertes relacionades amb aquest producte