SUNSET PAIN RELIEF - HEATING RELIEF- methyl salicylate stick

SUNSET PAIN RELIEF - HEATING RELIEF by

Drug Labeling and Warnings

SUNSET PAIN RELIEF - HEATING RELIEF by is a Otc medication manufactured, distributed, or labeled by SUNSET NOVELTIES, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Methyl Salicylate 10%

PURPOSE

Topical Analgesic.

USES:

Aid for temporary local relief of minor pain in muscles or joints

WARNINGS

For external use only.

WHEN USING

Use only as directed
Do not bandage tightly or use with a heating pad
Avoid contact with eyes and mucous membranes
Do not apply to wounds or damaged, broken or irritated skin
If you experience an allergic reaction, discontinue use and consult a doctor.

Do not expose the area treated with product to heat or direct sunlight.

FLAMMABLE:

Keep away from fire or flame.

IF PREGNANT OR BREAST – FEEDING:

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.

STOP USE AND ASK A DOCTOR IF:

Condition worsens
Redness is present
Irritation develops
Symptoms persist for more than 7 days or clear up occur again within a few days

You experience signs injury, such as pain, swelling or blistering where the product was applied.

DIRECTIONS:

Adults and Children over 12 years:

Apply a small amount on the area to be.
Massaged in a circular motion, let set for a few seconds.

Repeat as necessary, but no more than 3 to 4 times daily.

INACTIVE INGREDIENT

Cocos Nucifera Oil (Organic), Cetyl Esters, Tribehenin, Beeswax, Cannabis Sativa Seed Oil, Butyrospermum Parkii Butter, Cetyl Alcohol, Tocopherol, Eucalyptus Globulus Leaf Oil, Mentha Arvensis Herb Oil, Cannabidiol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Arnica Montana Flower Extract.

SUNSET - PAIN RELIEF + 500 CBD OIL HEATING RELIEF STICK

INGREDIENTS AND APPEARANCE

SUNSET PAIN RELIEF - HEATING RELIEF 
methyl salicylate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72937-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TRIBEHENIN (UNII: 8OC9U7TQZ0)
PEG-8 BEESWAX (UNII: 3C1QUF1TIR)
CETYL ESTERS WAX (UNII: D072FFP9GU)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
SHEA BUTTER (UNII: K49155WL9Y)
TOCOPHEROL (UNII: R0ZB2556P8)
CANNABIDIOL (UNII: 19GBJ60SN5)
TEA TREE OIL (UNII: VIF565UC2G)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
EUCALYPTUS OIL (UNII: 2R04ONI662)
COCONUT OIL (UNII: Q9L0O73W7L)
CETYL ALCOHOL (UNII: 936JST6JCN)
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)

Product Characteristics
Color	white (OFF WHITE)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72937-110-01	30 mL in 1 CYLINDER; Type 0: Not a Combination Product	09/08/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/08/2022

Labeler - SUNSET NOVELTIES, INC (067218145)