PLANTAR FASCIITIS CREAM- camphor cream

Plantar Fasciitis Cream by

Drug Labeling and Warnings

Plantar Fasciitis Cream by is a Otc medication manufactured, distributed, or labeled by SOLALIA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Camphor 5%

PURPOSE

Topical Analgesic

INDICATIONS & USAGE

- helps relieve minor foot and heel discomfort such as: arch tightness, stiffness, soreness linked to plantar fasciitis, ired or overused feet

WARNINGS

For external use, do not take orally or get into eyes

Do not use on open wounds.

• if there are abnormalities such as skin rashes and allergies, do not scratch.
• Avoid contact with eyes and mucous membranes

If you experience an allergic reaction, discontinue use and consult a physician

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

• Clean the affected area before use.
• Take an appropriate amount of this product and apply it evenly on the affected area, massage until completely absorbed.
• Adults and children 12+, apply to affected area up to 3-4 times daily.
• Children under 12, ask a doctor.

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Water, Glycerin, Angelica Sinensis Root, Taraxacum Officinale, Safflower, Black Pepper, Clove, Cinnamon, Cinnamomum Cassia Twig, Ligusticum Wallichii Root, Wormwood, Stearic Acid, Glyceryl Monostearate, Methylparaben, Phenoxyethanol, Borneol

QUESTIONS

please contact us at: scogurei@gmail.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PLANTAR FASCIITIS CREAM 
camphor cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85849-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR, (-)- (UNII: 213N3S8275) (CAMPHOR, (-)- - UNII:213N3S8275)	CAMPHOR, (-)-	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
TARAXACUM OFFICINALE (UNII: 39981FM375)
SAFFLOWER (UNII: 4VBL71TY4Y)
CLOVE (UNII: K48IKT5321)
CINNAMOMUM CASSIA TWIG (UNII: 4UD6VQR2UP)
WORMWOOD (UNII: F84709P2XV)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BORNEOL (UNII: M89NIB437X)
GLYCERIN (UNII: PDC6A3C0OX)
LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)
BLACK PEPPER (UNII: KM66971LVF)
CINNAMON (UNII: 5S29HWU6QB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85849-012-01	50 mL in 1 CARTON; Type 0: Not a Combination Product	07/18/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/18/2025

Labeler - SOLALIA LLC (060233478)