HIGHPOTHECARY THERAPEUTICS CBD ZING- menthol cream 
SIBORG LLC

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.

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Highpothecary Therapeutics CBD Zing

Drug Facts

Active ingredient

Menthol 1.25%

Purpose

Topical Analgesic

Use

Warnings

For external use only.

When using this product

  • avoid contact with the ey es
  • do not apply to wounds or damaged skin 
  • do not bandage tightly

Stop use and ask a doctor if

  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Protect this product from excessive heat and direct sunlight.

Inactive ingredients

Aqua (Deionized Water), Aminomethyl Propanol, Arnica Montana Flower Extract, Beta Caryophyliene, Cannabis Sativa Oil, Capric/Caprylic Triglyceride, Cetyl Alcohol, Chondroitin Sulfate, Dimethyl Sulfone (MSM), Emu Oil, Ethylhexylglycerin, Full Spectrum Hemp CBD Extract (Cannabidiol), Glucosamine Sulfate, Phenoxyethanol, Propylene Glycol, Steareth-2, Steareth-21, Stearic Acid, Stearyl Alcohol

Questions or Comments?

1-866-272-4425

Package Labeling:

Label14

HIGHPOTHECARY THERAPEUTICS CBD ZING 
menthol cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70803-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL12.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
EMU OIL (UNII: 344821WD61)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
CANNABIDIOL (UNII: 19GBJ60SN5)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARETH-2 (UNII: V56DFE46J5)  
STEARETH-21 (UNII: 53J3F32P58)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70803-001-8888.72 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/07/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/07/2020
Labeler - SIBORG LLC (102875148)
Registrant - Geo Management Corporation (102875148)

Revised: 7/2021
Document Id: c7d13b10-f220-5872-e053-2995a90a49d8
Set id: 01e9e289-e55a-4721-966b-26a89a2ed27b
Version: 3
Effective Time: 20210723
 
SIBORG LLC