Indications and uses
Temporarily relieves minor aches and pains of muscles and joints due to: • arthritis • simple backache • strains • bruises • sprains
Capsaicin Patch
- Manufacturer
- Beijing HKKY Medical Tech. Co., Ltd.
- Effective date
- 2020-07-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:19:50
Label at a glance#
ProductCapsaicin
Active ingredientCAPSAICIN
Label structure10 sections
Dosage and administration
Adults and children 18 years of age and older: Apply 1 patch to the affected area of intact skin up to 3 times a day. Do not leave patch on for more than 8 hours at a time. Instructions for Use: - Clean and dry the affected area. - Open pouch and remove one patch. - Remove any protective film and apply directly to affected area of pain. Apply immediately after removal from the protective envelope. - Wash hands wit...
Storage and handling
Store in a dry cool place
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
CAPSAICIN – Capsaicin 0.025% Patch
Drug Facts
Active ingredient
Capsaicin 0.025%
Purpose
External analgesic
Uses
Temporarily relieves minor aches and pains of muscles and joints due to:
• arthritis
• simple backache
• strains
• bruises
• sprains
Warnings
For external use only. Use only as directed or as directed by a health care professional
Read all warnings and directions before use.
Discontinue use at least one hour prior to bath, shower, or swimming; do not use immediately after bath, shower, or swimming.
Do not use
• On wounds, cuts, damaged or infected skin
• On eyes, mouth, genitals, or any other mucous membranes
Allergy Alert: if you are allergic to capsicum or chili peppers or any inactive ingredient of this product, contact a doctor before use.
When using this product
• You may experience a burning sensation. The intensity of this reaction varies among individuals and may be severe. With regular use, this sensation generally disappears after several days.
• Avoid contact with the eyes, lips, nose and mucous membranes
• Do not tightly wrap or bandage the treated area
• Do not apply heat to the treated area immediately before or after use
Stop use and ask a physician:
• If pregnant or breast feeding
• If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician.
• If severe burning persists or blistering occurs
Keep out of reach of children and pets.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Adults and children 18 years of age and older:
Apply 1 patch to the affected area of intact skin up to 3 times a day. Do not leave patch on for more than 8 hours at a time.
Instructions for Use:
- Clean and dry the affected area.
- Open pouch and remove one patch.
- Remove any protective film and apply directly to affected area of pain. Apply immediately after removal from the protective envelope.
- Wash hands with soap and water after handling the patches.
- Reseal pouch containing unused patches after each use. Do not store patch outside the sealed envelope.
-Discontinue use at least 1 hour before a bath or shower and do not use immediately after a bath or shower
- Fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get to them.
Children under 18 years: Ask a physician
Other information
Store in a dry cool place
PRECAUTIONS
Aqua (Deionized Water), Sodium Polyacrylate, Glycerin, Sorbitol, Sodium Cellulose Glycolate, Polysorbate 80, Lemon Oil, Aluminum Glycinate, Eucalyptus Oil, Methylparaben, EDTA Disodium Salt
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Capsaicin
- WATER
- SODIUM POLYACRYLATE (8000 MW)
- GLYCERIN
- SORBITOL
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
- POLYSORBATE 80
- LEMON OIL
- DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS
- EUCALYPTUS OIL
- METHYLPARABEN
- EDETATE DISODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71073-208 | 71073-208-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| SODIUM POLYACRYLATE (8000 MW) | 285CYO341L | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| SORBITOL | 506T60A25R | IACT |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM | K679OBS311 | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| LEMON OIL | I9GRO824LL | IACT |
| DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS | 1K713C615K | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| CAPSAICIN | S07O44R1ZM | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ab9f9354-c3c7-9538-e053-2a95a90a2efe | 2f26e2a1-5efc-4d40-a3e7-cc06c326103b | 2020-07-29 | Warnings | ab9f9354-c3c7-9538-e053-2a95a90a2efe 2f26e2a1-5efc-4d40-a3e7-cc06c326103b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.