NERVIVE PAIN RELIEVING LIQUID ROLL-ON- lidocaine hcl and menthol liquid

Nervive Pain Relieving by

Drug Labeling and Warnings

Nervive Pain Relieving by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Lidocaine HCl 4%

Menthol 1%

Active ingredients Purpose

Topical anesthetic

Topical analgesic

Use

temporarily relieves minor pain

Warnings

For external use only

Flammable

• keep away from heat and open flame

Do not use

If you have had an allergic reaction to lidocaine or other local anesthetics

on large areas of the body or on cut, irritated, blistered, or swollen skin

on puncture wounds

for more than one week without consulting a doctor

When using this product

use only as directed. Read and follow all directions and warnings on this carton.

avoid contact with eyes and mucous membranes

rare cases of serious burns have been reported with products of this type

do not apply to wounds or damaged, broken or irritated skin

do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use

a transient burning sensation may occur upon application but generally disappears in several days

avoid applying into skin folds

Stop use and ask a doctor if

condition worsens

severe burning sensation, redness, rash or irritation develops

symptoms persist for more than 7 days or clear up and occur again within a few days

you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

If pregnant or breast-feeding,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and pets.

OVERDOSAGE

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Shake well before use

adults and children over 12 years:

• apply a thin layer to affected area every 6 to 8 hours
• do not exceed 3 applications in a 24 hour period
• massage into painful area until thoroughly absorbed into skin

AFTER APPLYING, WASH HANDS WITH SOAP AND WATER
children 12 years or younger: ask a doctor

Store at no greater than 25°C (77°F).

Inactive ingredients

alcohol, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, carbomer homopolymer, ceteth-20 phosphate, cetearyl alcohol, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexyl glycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, phenoxyethanol, polysorbate 60, sorbitan isostearate, steareth-2, steareth-21, tocopherol, water

Questions?

1-855-446-4345

SPL UNCLASSIFIED SECTION

DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 2.5 OZ

NERVIVE™

PAIN RELIEVING

LIQUID ROLL-ON

LIDOCAINE HCl & MENTHOL

TARGETS MULTIPLE

NERVE PAIN RECEPTORS

MASSAGING ROLL-ON

NET WT 2.5 OZ (70.9 g)

INGREDIENTS AND APPEARANCE

NERVIVE PAIN RELIEVING  LIQUID ROLL-ON
lidocaine hcl and menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84126-317
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 g  in 100 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARETH-21 (UNII: 53J3F32P58)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
ISOHEXADECANE (UNII: 918X1OUF1E)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ALCOHOL (UNII: 3K9958V90M)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
POLYSORBATE 60 (UNII: CAL22UVI4M)
TOCOPHEROL (UNII: R0ZB2556P8)
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
STEARETH-2 (UNII: V56DFE46J5)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84126-317-03	1 in 1 CARTON	08/12/2024
1		70.9 g in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 84126-317-05	1 in 1 CARTON	03/18/2025
2		130.4 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/12/2024

Labeler - The Procter & Gamble Manufacturing Company (004238200)