Cold Hot Medicated Patch 5% Menthol
- Manufacturer
- Quality Choice | Foshan Aqua Gel Biotech Co., Ltd.,
- Effective date
- 2025-07-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 01:06:59
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENT
Active Ingredient ...............................................................................................Purpose
Menthol 5%...............................................................................................Topical Analgesic
INACTIVE INGREDIENT
CMC, dihydroxyaluminum aminoacetate, glycerin, kaolin, methylparaben, mineral oil, petrolatum, polyacrylic acid, polysorbate 80, propylene glycol, propylparaben, PVP, sodium polyacrylate, tartaric acid, titanium dioxide, water
KEEP OUT OF REACH OF CHILDREN
Do not use on infants. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away
INDICATIONS & USAGE
For temporary relief of minor aches and pains of muscles and joints: arthritis, simple backache, bursitis, tendonitis, cle strains, muscle sprains, bruises and cramps.
WARNINGS
For External Use Only.
DOSAGE & ADMINISTRATION
Adults and children 12 years of age and over: Clean and dry affected area, free of lotions, ointments and creams. Carefully remove backing from patch. Apply sticky side of patch to affected area. Do not use more than one patch in an 8 hour period. Repeat as necessary. Maximum 3 patches per day. Discard patch after single use. Reseal pouch after opening.
Children under 12 years of age: consult a physician.
PURPOSE
Topical Analgesic
When using this product
When using this product
■ Use only as directed
■ Rare cases of serious burns have been reported with products of this type
■Don't bandage tightly or use with heating pad
■ Avoid contact with eyes and mucous membranes
■ Don't apply to wounds or damaged skin
■ Do not use at the same time as other topical analgesics.
Stop use and ask a doctor
If condition worsens ■ If redness is present ■ If irritation develops
■ If symptoms persist for more than 7 days or clear up and occur again within a few days.
■ You experience signs injury, such a s pain, swelling, or blistering where the product was applied.
If pregnant or breastfeeding
ask a health professional before use.
Cold Hot Medicated Patch 5% Menthol
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83324-256-05 | Cold Hot Medicated Patch 5% Menthol | 1 in 1 POUCH | PATCH | 1 | 1 | |
| 83324-256-05 | Cold Hot Medicated Patch 5% Menthol | 5 in 1 BOX | PATCH | 5 | 1 |
Products#
Every source-derived product name is available through these pages.
- Cold Hot Medicated Patch 5% Menthol
- MENTHOL
- PETROLATUM
- MINERAL OIL
- WATER
- GLYCERIN
- SODIUM POLYACRYLATE (8000 MW)
- DIHYDROXYALUMINUM AMINOACETATE
- METHYLPARABEN
- PROPYLPARABEN
- TITANIUM DIOXIDE
- KAOLIN
- POLYSORBATE 80
- PROPYLENE GLYCOL
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
- TARTARIC ACID
- POVIDONE, UNSPECIFIED
- POLYACRYLIC ACID (8000 MW)
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 83324-256 | 83324-256-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| Cold Hot Medicated Patch 5% Menthol | MENTHOL | Quality Choice | ce544a7c-8dc6-4e63-b499-d8a4e0ec48c3 | 2025-07-10 | Warnings | 83324-256-05 83324-256 83324025605 39941719-aa89-f083-e063-6394a90ac064 ce544a7c-8dc6-4e63-b499-d8a4e0ec48c3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
