Label: ADVANCED NUMB TOPICAL ANESTHETIC- lidocaine hydrochloride cream
- NDC Code(s): 71131-052-02, 71131-052-04
- Packager: Uber Scientific, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 13, 2023
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- DRUG FACTS
- Active Ingredients
- Use
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Warnings
For external use only. If condition worsens or does not improve within 7 days, consult a doctor.
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Directions
Adults and children 12 years and older: For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a clean, soft cloth before application of this product.
Apply externally up to 6 times per day.
Children under 12: Consult a Doctor.
- Inactive ingredients
- Other Information
- Package Labeling:
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INGREDIENTS AND APPEARANCE
ADVANCED NUMB TOPICAL ANESTHETIC
lidocaine hydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71131-052 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 50 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BENZYL ALCOHOL (UNII: LKG8494WBH) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71131-052-02 57 g in 1 JAR; Type 0: Not a Combination Product 04/20/2018 12/31/2020 2 NDC:71131-052-04 114 g in 1 JAR; Type 0: Not a Combination Product 04/20/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 04/20/2018 Labeler - Uber Scientific, LLC (080459429)