SUNSET HEATING PAIN RELIEF ROLL-ON- camphor gel

SUNSET HEATING PAIN RELIEF ROLL-ON by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Camphor ………………………………...…………………………….…. 4%

PURPOSE

Topical Analgesic

USE

Aid for temporary local relief of minor pain in muscles and joints.

WARNINGS

For external use only. Ask a doctor
before use if you have redness over affected area.

WHEN USING

• Avoid contact with the eyes or mucous membranes.
• Do not apply to wounds or damaged skin.
• Do not apply to the irritated skin or if excessive irritation develops.
• Do not bandage.
• Do not use with heating pad or device.
• Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days.

PREGNANCY 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.

DIRECTIONS

Adults and Children over 12 years of age

● Apply a small amount on the affected area.

● Massage in circular motion, let set for a few seconds.

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

Children under 12 years of age: Do not use, consult a doctor

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled room temperature between 59°F-86° F (15°C-30° C).

INACTIVE INGREDIENT

Water (Aqua), Alcohol Denat, Ceteareth-25, Glycerin, Caprylic/Capric Triglyceride, Calendula Officinalis Extract, Cannabis Sativa Seed Oil, Carbomer, Sodium Hydroxide, Methyl Salicylate, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, FD&C Yellow #6 (CI 15985).

QUESTIONS OR COMMENTS?

Contact us +1 (888) 367-4916

SUNSET HEATING PAIN RELIEF ROLL-ON

INGREDIENTS AND APPEARANCE

SUNSET HEATING PAIN RELIEF ROLL-ON 
camphor gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72937-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETEARETH-25 (UNII: 8FA93U5T67)
SALICYLIC ACID (UNII: O414PZ4LPZ)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
CARBOMER 940 (UNII: 4Q93RCW27E)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SORBIC ACID (UNII: X045WJ989B)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYL SALICYLATE (UNII: LAV5U5022Y)
ALCOHOL (UNII: 3K9958V90M)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERIN (UNII: PDC6A3C0OX)

Product Characteristics
Color	orange	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72937-019-03	89 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/02/2025

Labeler - SUNSET NOVELTIES, INC (067218145)