CARELAND HYDROGEL PAIN RELIEF PATCHES- lidocaine, menthol patch

Careland Hydrogel Pain Relief Patches by

Drug Labeling and Warnings

Careland Hydrogel Pain Relief 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 ingredient

Lidocaine 4.0%

Menthol 1.0%

Purpose

Topical analgesic

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

Children 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,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 HYDROGEL PAIN RELIEF PATCHES 
lidocaine, menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75568-022
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)
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: 75568-022-01	1 in 1 BOX	08/10/2024
1		8 in 1 POUCH
1		3 g in 1 PATCH; 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)