HEMPCIN ADVANCED TOPICAL PAIN RELIEF CREAM- menthol cream

HEMPCIN Advanced Topical Pain Relief Cream by

Drug Labeling and Warnings

HEMPCIN Advanced Topical Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Pedicis Research, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts:

Active Ingredient:

Menthol 5%

Purpose

Pain Relieving Cream

Uses:

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

Warnings:

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:

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:

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:

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

Directions:

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:

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:

Call toll free 1-800-748-6539

Package Labeling:

INGREDIENTS AND APPEARANCE

HEMPCIN ADVANCED TOPICAL PAIN RELIEF CREAM 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51151-391
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CHINESE CINNAMON OIL (UNII: A4WO0626T5)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LAURETH-7 (UNII: Z95S6G8201)
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
TEA TREE OIL (UNII: VIF565UC2G)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51151-391-00	1 in 1 BOX	02/13/2023
1		60 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/13/2023

Labeler - Pedicis Research, LLC (078496974)