ADVANCED PAIN RELIEF CREAM WITH 5 % NATURAL MENTHOL- menthol cream

Advanced Pain Relief Cream With 5 % Natural Menthol by

Drug Labeling and Warnings

Advanced Pain Relief Cream With 5 % Natural Menthol by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient;

Menthol - 5%

PURPOSE

Purpose:

Topical analgesic

INDICATIONS & USAGE

Uses:

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

DO NOT USE

Do not use on wounds or damaged skin

WHEN USING

When using this product:

avoid contact with eyes

do not bandage tightl

STOP USE

Stop use and ask a doctor if

condition worsens

irritation occurs

symptoms persist for more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.

Children under 2 years: Do not use, consult a doctor.

OTHER SAFETY INFORMATION

Other Information:

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

Store in a cool, dry place away from light

INACTIVE INGREDIENT

Inactive ingredients:

Water (Aqua), Ethoxydiglycol, Coconut Alkanes, Helianthus Annuus (Suflower) Seed Oil, Glyceryl Stearate, Cetyl Esters, PEG-100 Stearate, Dimethicone, Stearic Acid, Ammonium Acryloyldimethyltaurate/VP Copolymer, Cetearyl Alcohol, Ceteareth-20, Phenoxyethanol, Steareth-20, Coco-Caprylate/Caprate, Glycerl Stearates, Caprylyl Glycol, Butyrospermum Parkii Nut Extract, Methyl Gluceth-20, Ethylhexylglycerin, Hexylene Glycol, Glycerin, Disodium EDTA, Amica Montana Flower Extract, Sodium Ascorbyl Phospahte, Aloe Barbadensis Leaf Juice, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Boswella Carterii (Frankincense) Oil, Mentha Piperita (Peppermint) Oil, Camphor, Limonene, Linalool, Alpha-Terpinene, Terpineol, Terpinolene, Pinene, Eugenol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ADVANCED PAIN RELIEF CREAM WITH 5 % NATURAL MENTHOL 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4278
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEG-100 STEARATE (UNII: YD01N1999R)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
ETHOXYDIGLYCOL (UNII: A1A1I8X02B)
DIMETHICONE (UNII: 92RU3N3Y1O)
STEARIC ACID (UNII: 4ELV7Z65AP)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
GLYCERIN (UNII: PDC6A3C0OX)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARETH-20 (UNII: YRC528SWUY)
LINALOOL, (+)- (UNII: F4VNO44C09)
COCONUT ALKANES (UNII: 1E5KJY107T)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
TERPINOLENE (UNII: N9830X5KSL)
BUTYROSPERMUM PARKII (SHEA) OIL (UNII: O88E196QRF)
BOSWELLIA CARTERII OIL (UNII: 67ZYA5T02K)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
CETYL ESTERS (UNII: D072FFP9GU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
TERPINEOL (UNII: R53Q4ZWC99)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
PINENE (UNII: 996299PUKB)
ALPHA-TERPINENE (UNII: I24X278AP1)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EUGENOL (UNII: 3T8H1794QW)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
STEARETH-20 (UNII: L0Q8IK9E08)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4278-2	1 in 1 CARTON	02/25/2026
1	NDC: 62742-4278-1	57 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	02/25/2026

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4278)