CAPSIMIDE- capsaicin 0.025% topical patch patch 
Sola Pharmaceuticals

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Capsimide Patch

Active Ingredients

Capsaicin 0.025%

Purpose

Topical Analgesic

Uses

Temporarily relieves minor pain.

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding

ask a health professional before use.

Keep our of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 12 years of age and over: Clean and dry affected area. Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Use one patch for up to 12 hours. Discard patch after single use. Children under 12 years of age: consuly a physician.

Other Information

Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

Other Ingredients

Glycerin, Sodium polyacrylate, Dihydroxyaluminum aminoacetate, Edetate disodium, Kaolin, Carboxymethylcellulose sodium, Titanium dioxide, L-Tartaric acid, Polyacrylic acid, Propylene glycol, Polysorbate 80, Isopropyl Myristate, Hydroxyacetophenone, Water, and PVP

Questions or comments?

866-747-7365

Manufactured for:

SOLA PHARMACEUTICALS LLC

Baton Rouge, LA 70810

www.solameds.us

Made in China

Capsimide Patch

NDC 70512-016-10

Qty: 10 Patches

(1 per pouch) x 10

Capsimide pouch

Capsimide box

CAPSIMIDE 
capsaicin 0.025% topical patch patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70512-016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.025 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
WATER (UNII: 059QF0KO0R)  
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
KAOLIN (UNII: 24H4NWX5CO)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
POVIDONE (UNII: FZ989GH94E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TARTARIC ACID (UNII: W4888I119H)  
POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
GLYCERIN (UNII: PDC6A3C0OX)  
Product Characteristics
Color    Score    
ShapeRECTANGLESize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70512-016-1010 in 1 BOX09/07/2022
19 g in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01709/07/2022
Labeler - Sola Pharmaceuticals (080121345)

Revised: 5/2024
Document Id: 18e5beac-7faf-80a4-e063-6294a90aa71f
Set id: e81c2de8-6429-d681-e053-2995a90a36a9
Version: 3
Effective Time: 20240520
 
Sola Pharmaceuticals