EQUATE BURN RELIEF- lidocaine hydrochloride gel

equate Burn Relief by

Drug Labeling and Warnings

equate Burn Relief by is a Otc medication manufactured, distributed, or labeled by Walmart Inc, Nantong Health & Beyond Hygienic Products Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Lidocaine HCI         0.5%

PURPOSE

Purpose

External analgesic

INDICATIONS & USAGE

Uses

for the temporary relief of pain and itching associated with 

• minor burns 
• sunburn 
• minor cuts 
• scrapes
• insect bites
• minor skin irritations

WARNINGS

Warnings

For external use only.

Do not use in large quantities, particularly over raw surfaces or blistered areas

When using this product avoid contact with eyes

Stop use and ask a doctorif condition worsens, or if symptoms persist for more than 7 days or clearup and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions 

• adults and children 2 years of age and older: apply to affected area no more than 3 to 4 times daily
• children under 2 years of age: ask a doctor

INACTIVE INGREDIENT

Inactive ingredients

Aloe Barbadensis Leaf Juice, Blue 1, Carbomer, Disodium EDTA, Ethylhexylglycerin, Glycerin, Maltodextrin, Menthol, Phenoxyethanol, Polysorbate 20, Propanediol, SD Alcohol, Sodium Hydroxide, Water, Yellow 5

PRINCIPAL DISPLAY PANEL

lebal

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE BURN RELIEF 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-237
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CARBOMER 934 (UNII: Z135WT9208)
DISODIUM HEDTA (UNII: KME849MC7A)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MENTHOL (UNII: L7T10EIP3A)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPANEDIOL (UNII: 5965N8W85T)
ALCOHOL (UNII: 3K9958V90M)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-237-08	226 g in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/15/2023

Labeler - Walmart Inc (051957769)

Establishment
Name	Address	ID/FEI	Business Operations
Nantong Health & Beyond Hygienic Products Inc.		421280161	manufacture(79903-237)