Centipaine for Pain Control

Centipaine for Pain Control by

Drug Labeling and Warnings

Centipaine for Pain Control by is a Otc medication manufactured, distributed, or labeled by ASCLEMED USA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CENTIPAINE FOR PAIN CONTROL- lidocaine 4%, menthol 1% patch 
ASCLEMED USA INC.

----------

Centipaine for Pain Control

Active Ingredients

Lidocaine 4%

Menthol 1%

Purpose

Topical Analgesic

Uses

For the temporary relief of pain.

Warnings

For external use only not intended for ingestion.

Do not use

• in large quantities, particularly over raw surfaces, or blistered areas.

When using this product

• Avoid contact with the eyes.

Stop use and ask doctor if

• condition worsens, or if symtoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

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

If pregnant or breast-feeding, ask a health professional before use.

Directions

• Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times a daily.
• Children under 2 years of age: consult a doctor.

Other Information

Store at 20-25 oC (68-77 oF) and protect from moisture.

Inactive ingredients

polyacrylamide, vinol, sodium polyacrylate; acrylate polymerization, purified water.

Questions?

(310) 320-0100

CENTIPAINE FOR PAIN CONTROL 
lidocaine 4%, menthol 1% patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76420-146
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	1 g  in 100 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
ETHENYL (UNII: PQ2K3G3591)
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76420-146-03	3 in 1 BOX	01/19/2022	04/27/2024
1		4 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	505G(a)(3)	12/23/2021	04/27/2024

Labeler - ASCLEMED USA INC. (059888437)

Revised: 4/2025

Document Id: 323e4375-7753-9124-e063-6394a90a1f28

34390-5

Set id: 1ccf0647-2b06-4466-940d-ff1019baeaf3

Version: 3

Effective Time: 20250408