Label: CAPSAICIN 0.025% CREAM- capsaicin 0.025% cream
- NDC Code(s): 59088-220-08
- Packager: Puretek Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 2, 2025
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- Official Label (Printer Friendly)
- Active Ingredients:
- Purpose:
- Uses
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Warnings:
For external use only
• This is not a face cream. Do not apply to the face.
• Do not use if allergic to chili peppers or if past allergic reaction to capsaicin.
• Do not apply to wounds or damaged, broken, sunburned, chapped or irritated skin.
• Do not bandage tightly.
• Do not apply within 1 hour before or after bath, shower, hot tub, sauna or vigorous exercise. Warm water,
perspiration or open pores can intensify the impact of this product and cause a burning sensation.
• Do not use with a heating pad, hot water bottle or other source of heat. Doing so can increase risk of serious
burns.When using this product
• Do not get into eyes and avoid contact with other mucous membranes. If contact occurs or if pain, discomfort or skin redness occurs, continually rinse with cool water and seek medical help.
If pregnant, breast-feeding or any medical conditions exist, ask a health professional before use. Keep out of reach of children and pets. if swallowed, get medical help or contact a Poison Control Center right away. If inhaled, remove to fresh air. If breathing is difficult, get medical attention immediately.
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Directions:
• Rotate pump’s spout counter-clockwise slightly to unlock; clockwise to lock.
• Before using on children under 18 years of age consult a physician.
• Apply sparingly to affected area not more than 4 times daily. However, for first use, apply to small area to test for sensitivity or skin reaction.
• Gently massage into the skin until fully absorbed.
• Wash hands with soap and water thoroughly after each application to avoid spreading to the eyes or other sensitive mucous membranes. - Other information
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Inactive ingredient
Acrylates Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis (Aloe Vera) Leaf Juice, Aqua (Purified Water), Arnica Montana Flower Extract, Ethyl Alcohol, Ethyl Menthane Carboxamide, Ethylhexylglycerin, Euterpe Oleracea (Acai) Fruit Oil, Glycerin, Hydroxyethyl Behenamidopropyl Dimonium Chloride, Lauryl Laurate, Linum Usitatissimum (Flax) Seed Oil, Mentha Piperita (Peppermint) Oil, Menthyl Lactate, Methyl Diisopropyl Propionamide, Phenoxyethanol, PPG-2 Hydroxyethyl Cocamide, Rosmarinus Officinals (Rosemary) Oil, Triethanolamine.
- Label
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INGREDIENTS AND APPEARANCE
CAPSAICIN 0.025% CREAM
capsaicin 0.025% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-220 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAPSICUM OLEORESIN (UNII: UW86K581WY) (CAPSICUM OLEORESIN - UNII:UW86K581WY) CAPSICUM OLEORESIN 0.025 mg in 1 g Inactive Ingredients Ingredient Name Strength ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H) GLYCERIN (UNII: PDC6A3C0OX) MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH) ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393) TRIETHANOLAMINE (UNII: 9O3K93S3TK) LAURYL LAURATE (UNII: GPW77G0937) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) ALCOHOL (UNII: 3K9958V90M) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X) AQUA (UNII: 059QF0KO0R) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) LINUM USITATISSIMUM (LINSEED) SEED OIL (UNII: 84XB4DV00W) METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489) PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X) HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH) EUTERPE OLERACEA FRUIT OIL (UNII: Z0W6766A2W) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-220-08 120 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/02/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 01/02/2025 Labeler - Puretek Corporation (785961046)

Manufactured in the USA by: