Label: DR. NUMB- lidocaine cream
- NDC Code(s): 69903-001-30
- Packager: Shinpharma Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 18, 2022
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- 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
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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 final part346 07/01/2016 Labeler - Shinpharma Inc (248552403) Registrant - Shinpharma Inc (248552403)