NUMBSKIN MAXIMUM STRENGTH PAIN RELIEVER- lidocaine cream

Numbskin Maximum Strength Pain Reliever by

Drug Labeling and Warnings

Numbskin Maximum Strength Pain Reliever by is a Otc medication manufactured, distributed, or labeled by Shinpharma Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Lidocaine 5%

Purpose

Anorectal (Hemorrhoidal)

Uses

For temporary relief of local discomfort, itching, soreness or burning in the perianal area associated with anorectal disorders

Warnings

For external use only

When using this product

• do not exceed the recommended daily dosage unless directed by a doctor
• do not put into the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

• allergic reaction occurs
• rectal bleeding occurs
• redness, irritation, swelling, pain or other symptoms begin or increase
• condition worsens or does not improve within 7 days

KEEP OUT OF REACH OF CHILDREN

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

Directions

• Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
• When first opening the tube, twist the cap and peel off the foil seal
• Apply externally to the affected area up to 6 times daily
• Children under 12 years: Consult a doctor

Other information

• always keep the tube tighlty closed
• store at temperatures not exceeding 59°F - 86°F (15°C-30°C)
• protect from freezing

Inactive ingredients

Benzyl Alcohol, Carbopol, Letcithin, Propylene Glycol, Tocopheryl Acetate, Water

Questions?

Contact our dedicated Customer Care at +1 (877) 786 2001 or email us at support@shinpharma.com

Principal Display Panel

NDC: 69903-007-02

Numbskin Maximum Strength Pain Reliever

INGREDIENTS AND APPEARANCE

NUMBSKIN MAXIMUM STRENGTH PAIN RELIEVER 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69903-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69903-008-30	1 in 1 CARTON	02/27/2025
1		60 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	02/27/2025

Labeler - Shinpharma Inc (248552403)