PAIN RESCUE- menthol cream

Pain Rescue by

Drug Labeling and Warnings

Pain Rescue by is a Otc medication manufactured, distributed, or labeled by SONORAN NUTRA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Purpose

Topical Analgesic

Warnings

Warnings: For external use only. Avoid contact with eyes, wounds, broken
skin or mucous membranes. Do not bandage tightly or use with heating pad.

Uses

Uses temporary relief of minor aches, muscles and joint pain associate with:
Arthritis Fibromyalgia Back, Neck, Shoulder, Leg, Hand and Foot Pain
Sports Injuries Stiffness Sprains Sciatica

Keep out of reach of children.

 If swallowed, seek medical help or contact Poison Control Center immediately. Children under 12 years of age, consult a
doctor. If pregnant or breastfeeding consult healthcare professional before use.

Directions

Apply liberally to the affected area, massage until well absorbed.

Use 3-4 times daily for a minimum initial period of 7-10 days for acute pain.

Use 2 times daily or as needed for chronic pain.

Let cream dry after application to prevent staining.

This product may cause an allergic reaction on some individuals.

Test on a small area before use. Store at room temperature.

Stop use

Stop Use if irritation occurs, condition worsens or lasts more than 7 days

Active ingredient

Menthol

Inactive Ingredient

Ingredients: Aloe Barbadensis (Aloe Vera Leaf Extract), Arnica
Montana Flower Extract, Boswellia Serrata (Frankincense) Oil, Capsaicin,
Dicaprylate/Caprylic Acids, Glucosamine, Helianthus Annuus (Sunflower) Seed
Oil, Hemp Seed Oil, Methylsulfonylmethane (MSM), Phenoxyethanol,
Rosmarinus Officinalis (Rosemary) Oil, Tridecth 6, Turmeric, Water (Aqua)

Pckage carton

INGREDIENTS AND APPEARANCE

PAIN RESCUE 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72648-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
FRANKINCENSE OIL (UNII: 67ZYA5T02K)
CAPSAICIN (UNII: S07O44R1ZM)
CAPRYLIC ACID (UNII: OBL58JN025)
GLUCOSAMINE (UNII: N08U5BOQ1K)
SUNFLOWER SEED OIL GLYCERETH-8 ESTERS (UNII: 358X17CAT0)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ROSMARINUS OFFICINALIS FLOWERING TOP OIL (UNII: OXN0D3N28L)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
TURMERIC (UNII: 856YO1Z64F)
WATER (UNII: 059QF0KO0R)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72648-100-01	60 g in 1 TUBE; Type 0: Not a Combination Product	11/06/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/06/2018

Labeler - SONORAN NUTRA LLC (080658393)

Establishment
Name	Address	ID/FEI	Business Operations
SONORAN NUTRA LLC		080658393	manufacture(72648-100)