Label: XCEPTOR CBD PAIN UNSCENTED- tea salicylate cream

  • 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 September 1, 2020

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS

    TEA SALICYLATE  10%

  • PURPOSE

    TOPICAL ANALGESIC

  • USES

    TOPICAL PAIN RELIEF FOR MINOR ACHES AND PAINS.

  • WARNINGS

    FOR EXTERNAL USE ONLY.

    KEEP AWAY FROM EYES.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • DIRECTIONS

    APPLY SMALL AMOUNT TO AFFECTED AREA AND RUB IN. ADD AS NEEDED.

  • OTHER INFORMATION

    STORE AT 20° - 25°C (68°-77°F)

  • INACTIVE INGREDIENTS

    ALOE BARBADENSIS LEAF JUICE EXTRACT, BENZOIC ACID, BENZYL ALCOHOL, BETA VULGARIS (BEET) ROOT EXTRACT, CANNABIDIOL FROM HEMP, COCOCAPRYLATE/CAPRATE, COCOS NUCIFERA (COCONUT) OIL, COCONUT ALKANES, CYCLODEXTRIN, DISTEARDIMONIUM HECTORITE, GLYCERIN, MAGNESIUM SULFATE, POLYGLYCERYL-3 DIISOSTEARATE, POLYGLYCERYL-3 POLYRICINOLEATE, SHEA BUTTER ETHYL ESTERS, SORBIC ACID, TREMELLA FUCIFORMIS SPOROCARP EXTRACT, XANTHAN GUM, WATER

  • QUESTIONS / COMMENTS?

    PLEASE CALL US AT (760) 710-0510

  • PRINCIPAL DISPLAY PANEL

    Xceptor_CBD Pain Cream_Unscented_LBL

  • INGREDIENTS AND APPEARANCE
    XCEPTOR CBD PAIN  UNSCENTED
    tea salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72519-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE10 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BEET (UNII: N487KM8COK)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    COCONUT ALKANES (UNII: 1E5KJY107T)  
    BETADEX (UNII: JV039JZZ3A)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)  
    SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG)  
    SORBIC ACID (UNII: X045WJ989B)  
    TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72519-102-2130 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product03/09/2019
    2NDC:72519-102-0115 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34810/04/2018
    Labeler - XCEPTOR LLC (081207471)