NERVIVE PAIN RELIEVING CREAM- lidocaine hcl and menthol cream

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%

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 and pets.

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

Directions

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

STORAGE AND HANDLING

Store at no greater than 25°C (77°F).

Inactive ingredients

acrylates/C10-30 alkyl acrylate crosspolymer, alcohol, aminomethylpropanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl
methicone, ceteth-20 phosphate, cetostearyl alcohol, dicetyl phosphate, dimethicone, edetate disodium, ethylhexylglycerin, glyceryl stearate, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, phenoxyethanol, polyoxyl 15 hydroxystearate, polysorbate 60, sorbitan isostearate, steareth-21, tocopherol, water

Questions?

1-855-446-4345

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 3.0 OZ

NERVIVE™

PAIN RELIEVING CREAM

LIDOCAINE HCl & MENTHOL

TARGETS MULTIPLE

NERVE PAIN RECEPTORS

PENETRATING CREAM

MEDICATED CREAM NET WT 3.0 OZ (85.1 g)

INGREDIENTS AND APPEARANCE

NERVIVE PAIN RELIEVING  CREAM
lidocaine hcl and menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84126-318
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
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
POLYSORBATE 60 (UNII: CAL22UVI4M)
TOCOPHEROL (UNII: R0ZB2556P8)
C30-45 ALKYL CETEARYL DIMETHICONE CROSSPOLYMER (UNII: 4ZK9VP326R)
POLYOXYL 15 HYDROXYSTEARATE (UNII: 71YMM1X75O)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
STEARETH-21 (UNII: 53J3F32P58)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
ISOHEXADECANE (UNII: 918X1OUF1E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ALCOHOL (UNII: 3K9958V90M)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84126-318-03	1 in 1 CARTON	08/12/2024
1		85.1 g in 1 TUBE; 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)