Chill Pain Away

Manufacturer
SOLITEINT Kozmetikum gyarto es forgalmazo, termelo es kereskedelmi Korlatolt Felelossegu Tarsasag | SOLITEINT Kozmetikum gyarto es forgalmazo termelo es kereskedelmi Korlatolt Felelossegu Tarsasag
Effective date
2022-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:43:41

Label at a glance#

ProductChill Pain Away
Active ingredientCAPSAICIN
Label structure12 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with: · arthritis ·simple backache · strains · sprains · bruises

Dosage and administration

Adults and children over 18 years: Apply to affected area. Massage into the painful area until thoroughly absorbed. Repeat as necessary but no more than 3 to 4 times daily. Wash hands with soap and water after applying. Children 18 years and younger: Consult doctor

Storage and handling

Store in a cool, dry place. Tamper-evident for your protection. Use only if safety seal is intact.

Label contents#

Full prescribing information#

Actve Ingredients

OTC - ACTIVE INGREDIENT SECTION

Capsaicin...0.025%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:

· arthritis ·simple backache · strains · sprains · bruises

WARNINGS SECTION

Use only as directed.

For external use only. Keep away from excessive heat or flame

OTC - WHEN USING SECTION

when using this product

  • avoid eye contact
  • do not apply to wounds or damaged skin
  • do no bandage tightly

OTC - STOP USE SECTION

Stop use and ask doctor if:

  • condition worsens
  • symptoms persist for more than 7 days, or clear up and reoccur again within a few days
  • redness is present
  • irritation develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask ahealth professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 18 years:

  • Apply to affected area. Massage into the painful area until thoroughly absorbed. Repeat as necessary but no more than 3 to 4 times daily.
  • Wash hands with soap and water after applying.

Children 18 years and younger:

  • Consult doctor

Other Information

STORAGE AND HANDLING SECTION

  • Store in a cool, dry place.
  • Tamper-evident for your protection. Use only if safety seal is intact.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Magnesium Chloride, Dimethyl Sulfone (MSM), Prunus Amygdalus Dulcis (Sweet Almond
Oil), Butyrospermum Parkii (Shea Butter), Sodium Lactate, Glyceryl Stearate, Undecane, Polygyceryl-6 Palmitate/Succinate, Pentene Glycol, Xylitylglucoside, Glyceryl Stearate Citrate, Glyceryl Stearate SE, Cetyl Palmitate, Cannabidiol Isolate, Anhydroxylitol, Xylitol, Cetearyl Alcohol, Tocopheryl Acetate (Vitamin E), Xanthan Gum, Tridecane, Sodium Chloride, Potassium Chloride, Magnesium Sulfate, Calcium Chloride, Ascorbyl Palmitate, Hydroxyacetophenone, Disodium EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75249-00475249-004-01, 75249-004-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f04b5bb1-4b0c-9501-e053-2995a90a72e6d7c778cd-8eb2-566e-e053-2995a90a41952022-12-20WarningsExact identifier
spl id: f04b5bb1-4b0c-9501-e053-2995a90a72e6
spl set id: d7c778cd-8eb2-566e-e053-2995a90a4195

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.