DR. NUMB- lidocaine cream

Dr. Numb by

Drug Labeling and Warnings

Dr. Numb by is a Otc medication manufactured, distributed, or labeled by Shinpharma Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Lidocaine 4% w/w

Purpose

Topical Anesthetic

Uses

Temporarily relieves pain and itching due to

• insect bites
• minor burns
• minor cuts
• minor scrapes
• minor skin irritations
• sunburn

Warnings

For external use only

When using this product

• avoid contact with the eyes
• do not use in large quantities, particularly over raw surfaces or blistered areas

Stop the use and consult doctor if

• allergic reaction occurs
• condition worsens or does not improve within 7 days
• symptoms clear up and return within a few days
• redness, irritation, swelling, pain or other symptoms begin or increase

keep out of reach of children

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

Directions

• Adults and children 2 years and older: Apply externally to the affected area up to 3 to 4 times a day
• Children under 2 years: Consult a doctor

Other information

• May be applied under occlusive dressing. 
• Store at 25 ̊C (77 ̊F);
• excursions permitted to 15-30 ̊C (59-86 ̊F) [see USP Controlled Room Temperature].

Inactive Ingredients

Benzyl Alcohol, Carbomer 934, Lecithin(Soybean), Propylene Glycol, Tocopheryl Acetate, Water.

Question or comments

Contact our dedicated Customer Care at +1(877) 786 2001 or email us at support@drnumb.com within 24 hours a day, from Monday to Saturday Pacific Time.

Principal Display Panel

NDC: 69903-003-30

Water-based, Hypoallergenic and Fast Penetrating Topical Pain Relief and Anti-Itch Formula

Apply to the skin to relieve pain

FOR EXTERNAL USE ONLY

Dr. Numb

TOPICAL ANESTHETIC CREAM

Lidocaine 4% Cream -  Topical Anesthetic

30g

INGREDIENTS AND APPEARANCE

DR. NUMB 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69903-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	1.2 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
CARBOMER 934 (UNII: Z135WT9208)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
PROPYLENE GLYCOL BUTYL ETHER (UNII: 6X8776AP5Z)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69903-003-30	1 in 1 CARTON	10/12/2017
1		30 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	10/12/2017

Labeler - Shinpharma Inc (248552403)

Registrant - Shinpharma Inc (248552403)