AFTER BURN- lidocaine hydrochloride gel

País: Estats Units

Idioma: anglès

Font: NLM (National Library of Medicine)

ingredients actius:

LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)

Disponible des:

Adventure Ready Brands

Vía de administración:

TOPICAL

tipo de receta:

OTC DRUG

indicaciones terapéuticas:

Topical Analgesic For the temporary relief of pain due to minor burns, sunburn, minor cuts, screapes or minor skin irritations - condition worsens - symptoms persist for more than 7 days or clear up and occur again within a few days

Estat d'Autorització:

OTC monograph not final

Fitxa tècnica

AFTER BURN- LIDOCAINE HYDROCHLORIDE GEL
ADVENTURE READY BRANDS
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
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AFTER BURN
ACTIVE INGREDIENT
Lidocaine Hydrochloride 2.50%
PURPOS E
Topical Analgesic
US ES
For the temporary relief of pain due to minor burns, sunburn, minor
cuts, screapes or minor skin
irritations
WARNINGS
For external use only.
WHEN USING THIS PRODUCT
avoid contact with eyes
do not use in large quantities, particularly over raw surfaces or
blistered areas
do not use longer than 1 week unless directed by a doctor
STOP USE AND ASK A DOCTOR IF
condition worsens
symptoms persist for more than 7 days or clear up and occur again
within a few days
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
IF IN EYES, flush with water for 15 minutes and call a doctor.
DIRECTIONS
Clean affected area
ADULTS AND CHILDREN 2 YEARS AND OLDER apply small amount to affected
area not more than 3 times daily
CHILDREN UNDER 2 YEARS consult a doctor.
INACTIVE INGREDIENTS
Aloe Vera gel, benzalkonium chloride, carbomer 980, glycerol USP,
herbal fragrance, menthol,
polysorbate 20, propylene glycol, purified water, and sodium hydroxide
(50%)
AFTER BURN
AFTER BURN
lidocaine hydrochloride gel
PRODUCT INFORMATION
Adventure Ready Brands
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:9 0 10 7-5120
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
LIDO CAINE HYDRO CHLO RIDE (UNII: V130 0 7Z41A) (LIDOCAINE -
UNII:9 8 PI20 0 9 8 7)
LIDOCAINE HYDROCHLORIDE
ANHYDROUS
25 mg
in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7)
CARBO MER HO MO PO LYMER TYPE C (UNII: 4Q9 3RCW27E)
GLYCERIN (UNII: PDC6 A3C0 OX)
MENTHO L (UNII: L7T10 EIP3A)
PO LYSO RBATE 2 0 (UNII: 7T1F30 V5Y