Label: DR. NUMB- lidocaine cream
- NDC Code(s): 69903-001-30
- 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
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Warnings
For external use only
When using this product
- do not exceed the recommended daily dosage unless directed by a doctor
- do not put into the rectum by using fingers or any mechanical device or applicator
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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 tissue or a soft cloth before application of product. Apply to the affected area upto 6 times a day
- Children under 12 years of age: Consult a doctor
- 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 tissue or a soft cloth before application of product. Apply to the affected area upto 6 times a day
- Other information
- Inactive Ingredients
- Question or comments
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
DR. NUMB
lidocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69903-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 1.5 g in 30 g Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL (UNII: LKG8494WBH) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PROPYLENE GLYCOL BUTYL ETHER (UNII: 6X8776AP5Z) TOCOPHERYL RETINOATE (UNII: 0WN694NBMM) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69903-001-30 1 in 1 CARTON 07/01/2016 1 30 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 07/01/2016 Labeler - Shinpharma Inc (248552403) Registrant - Shinpharma Inc (248552403)