MINTED LEAF ODORLESS HISTAMINE DHCL PAIN RELIEF AND HEMP EXTRACT- histamine dihydrochloride cream
MMG Consumer Brands, LLC

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MINTED LEAF Odorless Histamine DHCl Pain Relief + Hemp Extract

Drug Facts

Active ingredient

Histamine Dihydrochloride 0.03%

Purpose

Topical Analgesic

Indications

For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis
simple backache
sprains
bruises and strains.

Warnings:

For external use only.
Avoid contact with eyes.
If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children.

If swallowed, consult physician.

Do not apply

to wounds or damaged skin.

Do not bandage tightly.

If pregnant or breast feeding,

contact physician prior to use.

Directions

Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
Children under two-years of age: consult a physician.

Additional Information

Store at room temperature.

Other Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cannabis Sativa (Broad Spectrum Hemp) Oil, Caprylic/Capric Triglyceride, Cetearyl Olivate, Cetyl Alcohol, Citric Acid, Gluconolactone, Glycerin, Glyceryl Stearate, llex Paraguariensis (Yerba Mate’) Extract, Methylsulfonylmethane (MSM), Sodium Benzoate, Sorbitan Olivate, Xanthan Gum, Zemea (Corn) Propanediol.

Package Labeling:

Label

MINTED LEAF ODORLESS HISTAMINE DHCL PAIN RELIEF AND HEMP EXTRACT
histamine dihydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73102-061
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	0.3 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CANNABIS SATIVA WHOLE (UNII: B5ONF538PB)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CETYL ALCOHOL (UNII: 936JST6JCN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SORBITAN OLIVATE (UNII: MDL271E3GR)
XANTHAN GUM (UNII: TTV12P4NEE)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:73102-061-00	85 g in 1 JAR; Type 0: Not a Combination Product	08/01/2019	07/30/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M017	08/01/2019	07/30/2021

Labeler - MMG Consumer Brands, LLC (117036455)

Revised: 10/2023

Document Id: 08ee0969-39e5-0aa9-e063-6394a90aa96f

Set id: 216f098a-3acf-4ae5-a9bc-267445777ff0

Version: 3

Effective Time: 20231030

MMG Consumer Brands, LLC