Label: LIDOCAINE- maximum strength pain reliever cream
- NDC Code(s): 69903-005-05
- Packager: Shinpharma Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 3, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep Out Of Reach Of Children
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Directions
Adults and Children 12 years and older: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Apply to the affected area up to 6 times a day. Children under 12 years: Consult a doctor.
- Other Information
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
LIDOCAINE
maximum strength pain reliever creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69903-005 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 WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) LECITHIN, SUNFLOWER (UNII: 834K0WOS5G) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) BENZYL ALCOHOL (UNII: LKG8494WBH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69903-005-05 1 in 1 BOX 10/19/2021 1 50 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M015 10/19/2021 Labeler - Shinpharma Inc (248552403)