Dr. Hess Pain Relief by Natural Essentials, Inc. / NATURAL ESSENTIALS, INC. Drug Facts

Dr. Hess Pain Relief by

Drug Labeling and Warnings

Dr. Hess Pain Relief by is a Otc medication manufactured, distributed, or labeled by Natural Essentials, Inc., NATURAL ESSENTIALS, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. HESS PAIN RELIEF- menthol, unspecified form spray 
Natural Essentials, Inc.

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Drug Facts

Active Ingredient

Menthol 3.7%

Purpose

Topical Analgesic

Uses:

Relieves minor pain of muscles and joints associated with: arthritis, simple backache, strains, bruises, sprains.

Flammable:Do not use while smoking, or near heat or flame.

Do not use:In large quantities, particularly over raw surfaces or blisters.

When using this product:Keep out of eyes. Use only as directed. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

Stop use and ask a doctor:If condition worsens; symptoms persist for more than 7 days or clears up and occur again within a few days; need longer than a week.

If pregnant or breast-feeding:Ask a health professional before use.

Keep out of reach of children and pets:If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Shake well. Adults and children 12 years of age and older: spray product on area no more than 1 to 3 times daily. Children under 12 years of age: ask a doctor. Other information: May cause staining, use caution when spraying near fabric and unprotected surfaces.

Inactive ingredients:

Aloe Barbadensis Leaf Extract, *Arnica Extract, Camphor, *llex Paraguariensis Leaf Extract, SD Alcohol 39C, Tea Tree Oil, Tocopheryl Acetate (Vitamin E Acetate), Water. * Indicates Certified Organic

Principal Display Panel - 96 g Can Label

H ®

SINCE 1893

Dr+ Hess®

Pain Relief Spray

Menthol & Arnica Formula

ENRICHED WITH NATURAL INGREDIENTS
to help soothe sore muscles and joints

Net Wt 3.4oz. (96g)

DR. HESS PAIN RELIEF 
menthol, unspecified form spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66902-260
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	3.7 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ALCOHOL (UNII: 3K9958V90M)
TEA TREE OIL (UNII: VIF565UC2G)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66902-260-04	96 g in 1 CAN; Type 0: Not a Combination Product	01/26/2021	10/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/26/2021	10/08/2024

Labeler - Natural Essentials, Inc. (947484713)

Establishment
Name	Address	ID/FEI	Business Operations
NATURAL ESSENTIALS, INC.		947484713	manufacture(66902-260)

Revised: 10/2024

Document Id: 23f7fd42-4e64-b307-e063-6394a90a7c1d

34390-5

Set id: 952c72bf-5e63-4abf-9647-ef59b7d022cf

Version: 2

Effective Time: 20241008