Dr Saymans Wonder Rub

Dosage form: gel
Ingredients: LIDOCAINE HYDROCHLORIDE 40mg in 1g
Labeler: Sheffield Pharmaceuticals LLC
NDC code: 11527-384

Medically reviewed by Drugs.com. Last updated on Apr 17, 2024.

Drug Facts

Active ingredient

Lidocaine HCL 4%

Purpose

Topical anesthetic

Uses

Temporarily relieves minor pain

Warnings

For external use only

Do not use

on large areas of the body or on cut,irritated or swollen skin
on puncture wounds
for more than one week without consultanting a doctor

When using this product

use only as directed. Read and follow all directions and warnings on this carton.
do not allow contact with the eyes
do not bandage or apply local heat (such as heating pads) to the area of use.

Stop use and ask a doctor if

condition worsens
symptons persist for more than 7 days or clear up and occur again within a few days.

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

Keep this and all drugs out of the reach of children and pets.

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

Directions

Adults and children over 12 years:
apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period
Children under 12 years or younger: ask a doctor

Other information

Store at controlled room temperature 20°-25°C (68°-77°F)

Inactive Ingredients: Alcohol, Arnica Montana Extract, Cannabis Sativa Seed Oil, Cyclohexasiloxane, Cyclopentasiloxane, Glycerin, PEG/PPG-18/18 Dimethicone, Menthane Carboxamidoethyl Acetate, Phenoxyethanol, Potassium Hydroxide, Sodium Chloride, Water (purified)

Questions?(800)645-2158

Principal Panel-Tube

Dr Sayman Wonder Rub

Maximum Strength

4% Lidocaine

Pain Relieving

NET WT. 4.0 oz (113g)

Principal Panel - Carton

Dr.Sayman's Wonder Rub

Maximum Strength

4% Lidocaine

Pain Relieving

NET WT. 4.0 oz (113g)

DR SAYMANS WONDER RUB
lidocaine gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11527-384
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	40 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL
ARNICA MONTANA WHOLE
CANNABIS SATIVA SEED OIL
CYCLOMETHICONE 6
CYCLOMETHICONE 5
GLYCERIN
PEG/PPG-18/18 DIMETHICONE
N-((ETHOXYCARBONYL)METHYL)-P-MENTHANE-3-CARBOXAMIDE
PHENOXYETHANOL
POTASSIUM HYDROXIDE
SODIUM CHLORIDE
WATER

Packaging
#	Item Code	Package Description
1	NDC:11527-384-22	1 TUBE in 1 CARTON
1		113 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/21/2019

Labeler - Sheffield Pharmaceuticals LLC (151177797)

Registrant - Sheffield Pharmaceuticals LLC (151177797)

Establishment
Name	Address	ID/FEI	Operations
Sheffield Pharmaceuticals LLC		151177797	manufacture(11527-384)

Revised: 04/2020

Document Id: 745aa3e8-9a3c-4a8f-a3d5-0ceace4a75a2

Set id: 430d8a59-9b26-4d18-82f8-1a886b9399ad

Version: 1

Effective Time: 20200427

Sheffield Pharmaceuticals LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer