VELATRIN PAIN RELIEF- methyl salicylate, menthol, unspecified form cream

Velatrin Pain Relief by

Drug Labeling and Warnings

Velatrin Pain Relief by is a Otc medication manufactured, distributed, or labeled by Quality Nature, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients:

Methyl Salicylate 15.0%

Menthol 10.0%

Purpose:

Topical Analgesic

Uses:

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

Warnings:

For external use only. ​Allergy Alert:​ If you had prior allergic reaction to aspirin or salicylate, please consult a physician before use.

Do not use

on wounds or damaged skin with a heating pad. ​Ask a Physician before use if ​you have redness over the affected area.

When using this product

avoid contact with eyes and mucus membranes do not bandage tightly.

Stop use and ask a physician if

condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive skin irritation occur  pregnant or breastfeeding.

Keep out of reach of children.

In case of accidental ingestion, get medical help or contact a Poison Control Centre right away.

Directions:

Use only as directed 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 of age: consult a physician.

Other information:

Store at 20 °C to 25 °C (68 °F - 77 °F).

Inactive Ingredients:

Acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis (aloe vera gel) juice, aqua (deionized water), arnica montana (arnica) extract, camellia sinensis (green tea) leaf extract, citrus aurantium dulcis (orange) peel oil, citrus medica limonum (lemon) extract, ethylhexylglycerin, helianthus annuus (sunflower) seed oil, isopropyl myristate, PEG-8, phenoxyethanol, pyridoxine (vitamin B6), sodium lauryl sulfate, triethanolamine.

Package Labeling:

INGREDIENTS AND APPEARANCE

VELATRIN PAIN RELIEF 
methyl salicylate, menthol, unspecified form cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70287-716
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	15 mg  in 1 g
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA (UNII: O80TY208ZW)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
ORANGE OIL (UNII: AKN3KSD11B)
LEMON (UNII: 24RS0A988O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SUNFLOWER OIL (UNII: 3W1JG795YI)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PYRIDOXINE (UNII: KV2JZ1BI6Z)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70287-716-01	113 g in 1 JAR; Type 0: Not a Combination Product	02/09/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/25/2015

Labeler - Quality Nature, Inc. (080014569)