Label: PAIN RELIEVING GEL-PATCH- lidocaine patch
- NDC Code(s): 73557-159-01, 73557-159-06
- Packager: Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use ... if
- ... ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children
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Directions
Adult and Children 12 years of age and over:
- Clean and dry affected area
- Remove film from patch and apply to the skin (see illustration)
- Apply 1 patch at a time to affected area, not more than 3 to 4 times daily
- Remove patch from the skin after at most 8-hour application
Children under 12 years of age: Consult a doctor
- Dosage forms & strengths
- Other information
- Inactive Ingredients
- Questions or Comments
- Package label. Principal display panel
-
INGREDIENTS AND APPEARANCE
PAIN RELIEVING GEL-PATCH
lidocaine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73557-159 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 0.04 g in 1 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM (UNII: 7FLD91C86K) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) POLYSORBATE 80 (UNII: 6OZP39ZG8H) GLYCERIN (UNII: PDC6A3C0OX) POVIDONE K90 (UNII: RDH86HJV5Z) KAOLIN (UNII: 24H4NWX5CO) TARTARIC ACID (UNII: W4888I119H) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73557-159-06 6 in 1 BOX 11/01/2024 1 NDC:73557-159-01 12 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/01/2024 Labeler - Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (546872672) Registrant - Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (546872672) Establishment Name Address ID/FEI Business Operations Shanghai Chuangshi Medical Technology (Group) Co., Ltd. 546872672 manufacture(73557-159) , label(73557-159)