TETRACAINE gel

Riik: Ameerika Ühendriigid

keel: inglise

Allikas: NLM (National Library of Medicine)

Toimeaine:

TETRACAINE HYDROCHLORIDE (UNII: 5NF5D4OPCI) (TETRACAINE - UNII:0619F35CGV)

Saadav alates:

Bellus Medical, LLC

Manustamisviis:

TOPICAL

Retsepti tüüp:

OTC DRUG

Näidustused:

Topical Anesthetic Uses : For the temporary relief of discomfort and pain associated with - Minor burns and skin irritations - Minor cuts and scrapes - Itching Directions : Adults and Children 12 years of age and older Apply to affected area not more than 3-4 times daily.

Volitamisolek:

OTC monograph not final

Toote omadused

TETRACAINE- TETRACAINE GEL
BELLUS MEDICAL, LLC
----------
2% TETRACAINE GEL
Tetracaine HCL 2%
Water, Glycerin, Propylene Glycol, Hydroxyethyl Cellulose,
Phenoxyethanol, Caprylyl
Glycol, Aloe Barbadensis (Aloe Vera) Leaf Extract, Sorbic Acid,
Tetrasodium EDTA
USES : For the temporary relief of discomfort and pain associated with
Minor burns and skin irritations
Minor cuts and scrapes
Itching
DIRECTIONS : Adults and Children 12 years of age and older Apply to
affected area not
more than 3-4 times daily.
WARNINGS : For external use only. Avoid contact with the eyes.
DO NOT USE : In large quantities, particularly over raw surfaces and
blistered areas.
STOP USE AND ASK A DOCTOR IF:
Skin becomes irritated
Condition worsens or symptoms last more than 7 days
Symptoms clear up and reoccur within a few days.
Topical Anesthetic
Keep out of reach of children.
Uses : For the temporary relief of discomfort and pain associated with
Minor burns and skin irritations
Minor cuts and scrapes
Itching
Directions : Adults and Children 12 years of age and older Apply to
affected area not
more than 3-4 times daily.
TETRACAINE
tetracaine gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:71888-103
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
TETRACAINE HYDROCHLORIDE (UNII: 5NF5D4OPCI) (TETRACAINE -
UNII:0619F35CGV)
TETRACAINE
HYDROCHLORIDE
20 mg
in 1000 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EDETATE SODIUM (UNII: MP1J8420LU)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SORBIC ACID (UNII: X045WJ989B)
PACKAGING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
NDC:71888-103-
Bellus Medical, LLC
1
NDC:71888-103-
02
12 in 1 BOX
06/01/2017
1
NDC:71888-103-
01
4 mL in 1 PACKET; Type 0: Not a Combination
Product
MARKETING INFO