Label: UP AND UP LIDOCAINE PAIN RELIEF- lidocaine patch
- NDC Code(s): 11673-744-91
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 7, 2020
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
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- more than 1 patch at a time
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- on wounds or damaged skin
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- with a heating pad
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- if you have ever had an allergic reaction to this product or any of its ingredients
When using this product
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- use only as directed
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- avoid contact with the eyes, mucous membranes or rashes
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- do not bandage tightly
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Directions
Adults and children 12 years of age and over:
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- clean and dry affected area
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- remove film from patch and apply to the skin (see illustration)
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- apply 1 patch at a time to affected area, not more than 3 to 4 times daily
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- remove patch from the skin after at most 8 hours of application
Children under 12 years of age: consult a doctor
- Other information
- Inactive ingredients
- Questions?
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Principal Display Panel
Compare to active ingredient in Salonpas® & Aspercreme® Lidocaine Patch
up to 8 hours
maximum strength
lidocaine pain-relief patches
4% lidocaine/topical anesthetic
desensitizes aggravated nerves in back, neck, shoulders, knees and elbows
for temporary relief of pain
numbing
unscented
6 PATCHES
31 15/16 IN x 5 1/2 IN (10 cm x 14 cm) EACH
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INGREDIENTS AND APPEARANCE
UP AND UP LIDOCAINE PAIN RELIEF
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-744 Route of Administration TOPICAL, PERCUTANEOUS, TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 560 mg Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) KAOLIN (UNII: 24H4NWX5CO) METHYLPARABEN (UNII: A2I8C7HI9T) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) TARTARIC ACID (UNII: W4888I119H) UREA (UNII: 8W8T17847W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-744-91 6 in 1 CARTON 07/15/2019 1 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 07/15/2019 Labeler - Target Corporation (006961700)