ULTRA RELIEF- menthol, camphor gel

ULTRA RELIEF by

Drug Labeling and Warnings

ULTRA RELIEF by is a Otc medication manufactured, distributed, or labeled by CHEMCO CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Camphor 3%

Menthol 6%

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.
A transient burning sensation or redness may occur upon application but generally disappears in several days.
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.

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.

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 over 21 years:

Apply a small amount on the affected area.
Massage in circular motion, let set for a few seconds.
Repeat as neccesary, but no more than 3 to 4 times daily

Wash hands with soap and water after use.

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled room temperature between 59°-86° f (15°-30° c). This product is intended for use by healthy adults aged 21 years & older. consult a healthcare professional prior to use of full spectrum THC. Full spectrum THC may be harmful if you are pregnant, nursing or are taking any medication or have a medical condition.

INACTIVE INGREDIENT

Water (Aqua), Alcohol Denat, Propylene Glycol, Polysorbate 20, Glycerin, Carbomer, Sodium Hydroxide, Mentha Piperita (Peppermint) Oil, Rosmarinus Officinalis (Rosemary) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Thymus Vulgaris (Thyme) Oil, Cannabis Sativa Seed Oil, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, FD&C Yellow No.5 (CI 19140), FD&C Blue No.1 (CI 42090).

ULTRA RELIEF GEL

INGREDIENTS AND APPEARANCE

ULTRA RELIEF 
menthol, camphor gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49283-578
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	6 g  in 100 g
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
CARBOMER 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PEPPERMINT OIL (UNII: AV092KU4JH)
ROSEMARY OIL (UNII: 8LGU7VM393)
THYME OIL (UNII: 2UK410MY6B)
TEA TREE OIL (UNII: VIF565UC2G)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SORBIC ACID (UNII: X045WJ989B)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SALICYLIC ACID (UNII: O414PZ4LPZ)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Product Characteristics
Color	turquoise	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49283-578-04	113 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/15/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/15/2026

Labeler - CHEMCO CORPORATION (032495954)