Label: DERMFREE TATTOO NUMBING- lidocaine5% tattoo numbing cream
- NDC Code(s): 84010-020-01
- Packager: Jiangxi Hemei Pharmaceutical Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 4, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When Using
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Stop Use
Do not exceed the recommended daily dosage unless directed by a doctor.
Avoid contact with eyes. lf this happens, rinse thoroughly with water.
lf symptoms persist for more than 7 days or subside but occur again within 3 days, stop use and consult a physician.
Stop use and seek medical attention if signs of an allergy occur, such as redness,iritation, sweling, pain, or other severe symptoms. fsymptoms do not subside completely within 7 days, seek medica help.
- Ask Doctor
- Keep Oot Of Reach Of Children
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Directions
Before applying the numbing cream, thoroughly wash your hands and wear disposable tattoo gloves.
Clean the area of the body receivina the tattoo,Dry completely.
Apply a generous amount of numbing cream to the cleaned area and rub it inthoroughly in a circlar motion for30 to 60 seconds,Then. cover with plastic wrap.
Leave the cream and wrap in place for 30 to 45 minutes,Wipe away the cream and thoroughly clean the area to prepare for a pain-free tattoo.
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DERMFREE TATTOO NUMBING
lidocaine5% tattoo numbing creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84010-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 5 g in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SOYBEAN LECITHIN (UNII: 1DI56QDM62) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) BENZYL ALCOHOL (UNII: LKG8494WBH) CARBOMER 934 (UNII: Z135WT9208) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84010-020-01 20 g in 1 BOTTLE; Type 0: Not a Combination Product 08/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 08/15/2024 Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056) Establishment Name Address ID/FEI Business Operations Jiangxi Hemei Pharmaceutical Co., Ltd 724892056 manufacture(84010-020)