Label: NERVIVE PAIN RELIEVING LIQUID ROLL-ON- lidocaine hcl and menthol liquid
- NDC Code(s): 84126-317-03
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 6, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Use
- Warnings
- Do not use
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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
- If pregnant or breast-feeding,
- KEEP OUT OF REACH OF CHILDREN
- OVERDOSAGE
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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 doctorStore at no greater than 25°C (77°F).
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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?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 2.5 OZ
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INGREDIENTS AND APPEARANCE
NERVIVE PAIN RELIEVING LIQUID ROLL-ON
lidocaine hcl and menthol liquidProduct 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) 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) 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 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)