HEMP MAGIC FAST-ACTING PAIN RELIEF CREAM- menthol cream

Hemp Magic Fast-Acting Pain Relief Cream by

Drug Labeling and Warnings

Hemp Magic Fast-Acting Pain Relief Cream by is a Otc medication manufactured, distributed, or labeled by Nexxus Capital LLC, Epic Laboratories LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Mentha Arvensis (Menthol) 3%

PURPOSE

Purpose
Topical analgesic

INDICATIONS & USAGE

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

WARNINGS

Warnings

For external use only.

Avoid contact with eyes

Flammable:

keep away from fire or flame

- use only as directed

- do not bandage tightly or use with heating pad

- do not apply to wounds or damaged skin

Stop use and ask doctor if
- condition persist for more than 7 days or worsen, symptoms clear up and occur again within a few days

- redness is present

- excessive irritation of the skin develops

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

DOSAGE & 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 age: Consult a doctor.

INACTIVE INGREDIENT

Turmeric, Arnica, Aloe Barbadensis Leaf Juice, Capric/Caprylic Triglycerides, Glycerin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyltaurate Copolymer, Butyrospermum Parkii (Shea Butter), Phenoxyethanol, Xylitylglucoside, Anhydroxylitol, Mentha Piperita (Peppermint) Oil, Cannabis Sativa (Hemp) Seed Oil, Xylitol, Ethylhexylglycerin, Glucose, Polysorbate 60, Sorbitan Isostearate, Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEMP MAGIC FAST-ACTING PAIN RELIEF CREAM 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85294-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
CURCUMA LONGA (TURMERIC) ROOT (UNII: 856YO1Z64F)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYSORBATE 60 (UNII: CAL22UVI4M)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
WATER (UNII: 059QF0KO0R)
XYLITOL (UNII: VCQ006KQ1E)
SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
ARNICA MONTANA (UNII: O80TY208ZW)
DEXTROSE (UNII: IY9XDZ35W2)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85294-001-01	57 g in 1 JAR; Type 0: Not a Combination Product	02/17/2026
2	NDC: 85294-001-02	113 g in 1 JAR; Type 0: Not a Combination Product	02/17/2026
3	NDC: 85294-001-03	227 g in 1 JAR; Type 0: Not a Combination Product	02/17/2026
4	NDC: 85294-001-04	454 g in 1 JAR; Type 0: Not a Combination Product	02/17/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/17/2026

Labeler - Nexxus Capital LLC (085559168)

Registrant - Nexxus Capital LLC (085559168)

Establishment
Name	Address	ID/FEI	Business Operations
Epic Laboratories LLC		119307904	manufacture(85294-001)