Label: QC ARTHRITIS PAIN RELIEF- capsaicin liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63868-203-40 - Packager: Chain Drug Marketing Association Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 6, 2018
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
Directions
- adults and children 18 years of age and older:
- use only as directed
- clean and dry affected area
- place applicator on skin, press firmly and hold to activate the dispensing of liquid
- massage into painful area until thoroughly absorbed
- repeat as necessary, but no more than 3 to 4 times daily
- IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATER
- children under 18 years of age: ask a doctor
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
QC ARTHRITIS PAIN RELIEF
capsaicin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN 0.0015 g in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALCOHOL (UNII: 3K9958V90M) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-203-40 1 in 1 BOX 11/06/2018 1 40 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/06/2018 Labeler - Chain Drug Marketing Association Inc. (011920774)