HempCin Pain Relief Cream

Manufacturer
Pedicis Research, LLC
Effective date
2022-01-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:16:53

Label at a glance#

ProductHempCin Pain Relief
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

For the temporary relief of minor aches and pain of muscles and joints

Dosage and administration

Adults or children 2 years of age and older. Apply externally to affected area not more than 3-4 times daily. Children under 2 years of age consult a doctor

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

Purpose

OTC - PURPOSE SECTION

Pain Relieving Cream

Uses:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pain of muscles and joints

Warnings:

WARNINGS SECTION

  • For External Use only
  • Avoid contact with the eyes 
  • Do not apply to wounds or damaged skin 
  • Do not bandage tightly
  • Cap tube tightly and store at room temperature away from heat

When using this product:

OTC - WHEN USING SECTION

  • do not use in large quantities particularly over raw surfaces or blistered areas
  • do not exceed recommended doses unless recommended by a doctor

Stop use and ask a doctor if:

OTC - STOP USE SECTION

  • allergic reaction occurs 
  • condition worsens or does not improve within 7 days
  • symptoms clear up and do not return within a few days
  • you notice any unusual effects

Keep out of the reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or call a Poison Control Center right away

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Adults or children 2 years of age and older. Apply externally to affected area not more than 3-4 times daily.
  • Children under 2 years of age consult a doctor

Other Ingredients:

INACTIVE INGREDIENT SECTION

Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cannabis Sativa (Hemp) Seed Oil, Cassia Oil, Cetearyl Alcohol, Dimethyl Sulfone (DMSO), Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Ilex Paraguariensis (Yerba Mate’) Extract, C13-14 Isoparaffin, Isopropyl Alcohol, Laureth-7, Magnesium Sulfate, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Sodium Polyacrylate, Stearic Acid, Triethanolamine

Questions:

OTC - QUESTIONS SECTION

Call toll free 1-800-748-6539

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51151-12951151-129-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

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
d58dd679-491f-3187-e053-2a95a90af875e2755852-f27e-44bf-bcdd-64b69aea844d2022-01-14WarningsExact identifier
spl id: d58dd679-491f-3187-e053-2a95a90af875
spl set id: e2755852-f27e-44bf-bcdd-64b69aea844d

Reported adverse events (FAERS/openFDA)#

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