CARELAND LIDOCAINE PAIN RELIEVING- lidocaine patch

Drug Labeling and Warnings

Drug Details [pdf]

DRUG FACTS

Active ingredient

Lidacaine 4.0%

Purpose

Topical anesthetic

Use

For temporary relief 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 reations, 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

INACTIVE INGREDIENTS

Propylene Glycol, PEG-40 Hydrogenated Castor Oil, Vanillyl Butyl Ether, Phenoxyethanol,3-2-(Ethylhexyl)oxyl-1,2-PropandioI, Glycerol, Azone, a-Tocopherol Acetate, Sodium Polyacrylate, Dihydroxyaluminum Aminoacetate, CMC-2Na, Titanium Dioxide, Fumed Silica, Tartaric Acid, Polyacrylic Acid, Urea, Water

QUESTIONS?

626-839-9001 Service@getcareland.com

Package Labeling:

INGREDIENTS AND APPEARANCE

CARELAND LIDOCAINE PAIN RELIEVING 
lidocaine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75568-046
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

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
LAUROCAPRAM (UNII: 1F3X9DRV9X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TARTARIC ACID (UNII: W4888I119H)
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75568-046-00	15 in 1 BAG	04/15/2026
1		13 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	04/15/2026

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

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

Establishment
Name	Address	ID/FEI	Business Operations
Planet (Anhui) Pharmaceutical Co., Ltd.		618456104	manufacture(75568-046)