FDA.reportPublic FDA data

Hypothecary Therapeutics

Manufacturer
SIBORG LLC | Geo Management Corporation
Effective date
2021-07-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:41:37

Label at a glance#

ProductHighpothecary Therapeutics CBD Zing
Active ingredientMENTHOL
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • 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

OTC - STOP USE SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

SPL UNCLASSIFIED SECTION

Protect this product from excessive heat and direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

1-866-272-4425

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label14Label14

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70803-001-882023-01-30C16284748780-1c7ccaba7-1134-fd44-e053-dadaa90aa01bHighpothecary Therapeutics CBD Zing
70803-001-882021-07-23C16284748780-1c7ccaba7-1134-fd44-e053-dadaa90aa01bHighpothecary Therapeutics CBD Zing

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70803-001-88Highpothecary Therapeutics CBD Zing88.72 mL in 1 BOTTLE, PUMPCREAM88.723

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70803-001HIGHPOTHECARY THERAPEUTICS CBD ZING (MENTHOL) CREAM [SIBORG LLC]3Legacy NDC, 1 package rows20210724_01e9e289-e55a-4721-966b-26a89a2ed27b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70803-00170803-001-88

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
EMU OIL344821WD61IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CANNABIDIOL19GBJ60SN5IACT
GLUCOSAMINE SULFATE1FW7WLR731IACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
STEARIC ACID4ELV7Z65APIACT
STEARYL ALCOHOL2KR89I4H1YIACT
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c7d13b10-f220-5872-e053-2995a90a49d801e9e289-e55a-4721-966b-26a89a2ed27b2021-07-23WarningsExact identifier
spl id: c7d13b10-f220-5872-e053-2995a90a49d8
spl set id: 01e9e289-e55a-4721-966b-26a89a2ed27b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.