Label: CBD PAIN RELIEF CREAM- trolamine salicylate cream
- NDC Code(s): 62742-4198-1
- Packager: Allure Labs 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 December 17, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- ASK DOCTOR
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Inactive Ingredients: Water (Aqua), Coconut Alkanes*, Sorbitan Olivate*, Cetearyl Olivate*, Glycerin*, Dimethyl Sulfone, Glyceryl Stearate*,Cannabidiol (From Hemp Extract), Stearic Acid*, Cetyl Palmitate*, Rosa Moschata Seed Oil*, Cetearyl Alcohol, Ceteareth-20, Sorbitan Palmitate*, Tocopherol, Vanillyl Butyl Ether, Coco-Caprylate/Caprate*, Caprylhydroxamic acid*, Glyceryl Caprylate*, Xanthan Gum*
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CBD PAIN RELIEF CREAM
trolamine salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4198 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE 100 mg in 1 g Inactive Ingredients Ingredient Name Strength CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) COCONUT ALKANES (UNII: 1E5KJY107T) CANNABIDIOL (UNII: 19GBJ60SN5) ROSA MOSCHATA SEED OIL (UNII: T031ZE559T) VANILLYL BUTYL ETHER (UNII: S2ULN37C9R) WATER (UNII: 059QF0KO0R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) TOCOPHEROL (UNII: R0ZB2556P8) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) SORBITAN OLIVATE (UNII: MDL271E3GR) GLYCERIN (UNII: PDC6A3C0OX) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) CETEARYL OLIVATE (UNII: 58B69Q84JO) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) SORBITAN MONOPALMITATE (UNII: 77K6Z421KU) XANTHAN GUM (UNII: TTV12P4NEE) STEARIC ACID (UNII: 4ELV7Z65AP) CETYL PALMITATE (UNII: 5ZA2S6B08X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4198-1 57 g in 1 TUBE; Type 0: Not a Combination Product 12/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 12/17/2020 Labeler - Allure Labs Inc (926831603) Registrant - Allure Labs Inc. (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs Inc 926831603 manufacture(62742-4198)