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Drug Facts
DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202
Nervive Pain Relieving Liquid
FDA Label NDC 84126-317
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Procter & Gamble Manufacturing Company for the product Nervive Pain Relieving (NDC 84126-317). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredients, active ingredients purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Otc - 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
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)
317 (317)
* Please review the disclaimer below.
