Hemp Magic Fast-Acting Pain Relief Cream

Manufacturer
Nexxus Capital LLC | Epic Laboratories LLC
Effective date
2026-02-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:49:05

Label at a glance#

ProductHemp Magic Fast-Acting Pain Relief Cream
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient
Mentha Arvensis (Menthol) 3%

OTC - PURPOSE SECTION

Purpose
Topical analgesic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Warnings

For external use only.

SPL UNCLASSIFIED SECTION

Avoid contact with eyes

Flammable:

SPL UNCLASSIFIED SECTION

keep away from fire or flame

OTC - WHEN USING SECTION

- use only as directed

- do not bandage tightly or use with heating pad

- do not apply to wounds or damaged skin

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

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 age: Consult a doctor.

INACTIVE INGREDIENT SECTION

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.

RECENT MAJOR CHANGES 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 age: Consult a doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hemp Magic Fast-Acting Pain Relief Cream Menthol 3% Topical Analgesic Net Wt 2 oz (57 g)Hemp Magic Fast-Acting Pain Relief Cream Menthol 3% Topical Analgesic Net Wt 2 oz (57 g)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85294-001-01Hemp Magic Fast-Acting Pain Relief Cream57 g in 1 JARCREAM571
85294-001-02Hemp Magic Fast-Acting Pain Relief Cream113 g in 1 JARCREAM1131
85294-001-03Hemp Magic Fast-Acting Pain Relief Cream227 g in 1 JARCREAM2271
85294-001-04Hemp Magic Fast-Acting Pain Relief Cream454 g in 1 JARCREAM4541

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85294-00185294-001-01, 85294-001-02, 85294-001-03, 85294-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
Hemp Magic Fast-Acting Pain Relief CreamMENTHOLNexxus Capital LLC4af69640-1413-868b-e063-6394a90a39892026-02-16WarningsExact identifier
ndc (package): 85294-001-01
ndc (package): 85294-001-03
ndc (package): 85294-001-04
ndc (package): 85294-001-02
ndc (product): 85294-001
ndc11 (package): 85294000104
ndc11 (package): 85294000101
ndc11 (package): 85294000102
ndc11 (package): 85294000103
spl id: 4af69640-1414-868b-e063-6394a90a3989
spl set id: 4af69640-1413-868b-e063-6394a90a3989

Reported adverse events (FAERS/openFDA)#

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