NUNATURE FIRST AID GEL- lidocaine hci/benzethonium chloride gel

NuNature First Aid Gel by

Drug Labeling and Warnings

NuNature First Aid Gel by is a Otc medication manufactured, distributed, or labeled by Tec Laboratories Inc, Tec Laboratories Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzethonium Chloride 0.2%

Lidocaine Hydrochloride 2.5%

INDICATIONS & USAGE

Uses

• ​​​First aid to help prevent infection in minor:
• cuts
• scrapes
• burns
• For the temporary relief of pain or discomfort in minor:
• cuts
• scrapes
• burns

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

• in large quantitiies particularly over raw surfaces or blister areas

WHEN USING

When using this product

avoid contact with eyes

STOP USE

Stop use and ask a doctor if

• symptoms last for more than 7 days or clear up and occur again within a few days
• conditions worsens

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

if swallowed, get medical help or contact Poison Control center right away

DOSAGE & ADMINISTRATION

Directions

• adults and children 2 years of age and older:clean the affected area whenever possible
• apply to affected area not more than 3 to 4 times daily
• may be covered with a sterile bandange;if bandaged, let dry first
• children under 2 years of age:do not use, consult a doctor

STORAGE AND HANDLING

Other information

Store at 59-86ºF(15-30ºC)

INACTIVE INGREDIENT

allantoin, aminomethyl propanol, carbomer, disodium EDTA, glycerin, polyoxyl 35 castor oil, purified water, sodium carbonate, sodium metabisulfite, tea tree oil, white thyme oil.

QUESTIONS

Questions?

Call 1-800-482-4464.Serious side effects associated with this product may be reported to this number.

PURPOSE

Topical Analgestic and First Aid Antiseptic

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NUNATURE FIRST AID GEL 
lidocaine hci/benzethonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51879-211
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	2 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	25 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
THYME OIL (UNII: 2UK410MY6B)
ALLANTOIN (UNII: 344S277G0Z)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
POLYOXYL 35 CASTOR OIL (UNII: 6D4M1DAL6O)
SODIUM CARBONATE (UNII: 45P3261C7T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51879-211-01	28.3 g in 1 TUBE; Type 0: Not a Combination Product	08/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/11/2022

Labeler - Tec Laboratories Inc (083647792)

Establishment
Name	Address	ID/FEI	Business Operations
Tec Laboratories Inc		083647792	manufacture(51879-211)