CARELAND PLANTAR FASCIITIS HYDROGEL PAIN PATCHES- lidocaine, menthol patch

Careland Plantar Fasciitis Hydrogel Pain Patches by

Drug Labeling and Warnings

Careland Plantar Fasciitis Hydrogel Pain Patches by is a Otc medication manufactured, distributed, or labeled by Planet (Anhui) Pharmaceutical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active ingredients

Lidocaine 4.0%
Menthol 1.0%

Purpose

Topical anesthetic

Use

For temporary relief of pain

WARNINGS

For external use only

Do not use

• more than 1 patch at a time
• on wounds or damaged skin
• with a heating pad
• if you are allergic to any ingredients of this product

When using this product

• use only as directed
• do not bandage tightly
• avoid contact with the eyes, mucous membranes or rashes

Stop use and ask a doctor if

• symptoms persist for more than 7 days
• conditions worsen
• symptoms clear up and occur again within a few days
• localized skin reactions, such as rash, itching, redness, pain, swelling and blistering develop

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.

DIRECTIONS

Adults and children 12 years of age and over:

• clean and dry affected area
• remove film from patch and apply to the skin
• apply 1 patch at a time to affected area, not more than 3 to 4 times daily

Chidren under 12 years of age:consult a doctor

OTHER INFORMATION

• Store in a clean, dry place outside of direct sunlight. Protect product from excessive moisture

INACTIVE INGREDIENTS

Azone,Castor oil,Dihydroxyaluminum Aminoacetate,Disodium edetate dihydrate,Fumed silica,Glycerol,Isopropyl Myristate, Polyacrylic Acid, Polysorbate 80,Propylene Glycol,Sodium Polyacrylate, Tartaric Acid,Titanium Dioxide,Urea,water

QUESTIONS?

1-888-655-1558 Service@getcareland.com

Package Labeling:

INGREDIENTS AND APPEARANCE

CARELAND PLANTAR FASCIITIS HYDROGEL PAIN PATCHES 
lidocaine, menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75568-017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LAUROCAPRAM (UNII: 1F3X9DRV9X)
CASTOR OIL (UNII: D5340Y2I9G)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TARTARIC ACID (UNII: W4888I119H)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75568-017-01	8 in 1 BOX	08/10/2024
1		3 g in 1 POUCH; Type 0: Not a Combination Product

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

Labeler - Planet (Anhui) Pharmaceutical Co., Ltd. (618456104)

Establishment
Name	Address	ID/FEI	Business Operations
Planet (Anhui) Pharmaceutical Co., Ltd.		618456104	manufacture(75568-017)