HYPOTHECARY THERAPEUTICS- menthol cream

Highpothecary Therapeutics CBD Zing by

Drug Labeling and Warnings

Highpothecary Therapeutics CBD Zing by is a Otc medication manufactured, distributed, or labeled by SIBORG LLC, Geo Management Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Menthol 1.25%

Purpose

Topical Analgesic

Use

• For the temporary relief of minor aches and pains of muscles and joints.

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

• Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.
• Children under 12 years of ag e: Consult a doctor

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:

INGREDIENTS AND APPEARANCE

HYPOTHECARY THERAPEUTICS 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70803-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	12.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70803-001-88	88.72 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/07/2020

Labeler - SIBORG LLC (102875148)

Registrant - Geo Management Corporation (102875148)