VAGI-CURE (REGULAR STRENGTH)

Dosage form: cream
Ingredients: BENZOCAINE 50mg in 1g, BENZALKONIUM CHLORIDE .13mg in 1g
Labeler: SCI International, Inc. DBA Continental Pharmaceuticals
NDC code: 76466-075

Medically reviewed by Drugs.com. Last updated on Jan 14, 2025.

Directions:

Apply liberally to affected area. If needed may be repeated three top four times daily. Children under (2) two years of age: Consult a physician.

Active ingredients:

Aloe Vera Gel, Carbomer, Cetyl Alcohol, De-ionized Water, Disodium EDTA, Fragrance, Glycerol Monostearate, Isopropyl Myristate, Isopropyl Palmitate, Lanolin Anhydrous, Methylparaben, Mineral Oil, Peg 100 Stearate, propylene Glycol, Propylparaben, Vitamin E (tocopherol)

Warnings:

FOR EXTERNAL USE ONLY. Avoid contact with eyes.

Stop use and ask doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days.

Do not use if you have an unusual or abnormal vaginal discharge except under the supervision of a physician. Do not apply over large areas of the body.

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Store at 15 to 30C (49 to 85F)

Manufactured for:
Continental Pharmaceutical Inc.
5904 Enterprise Court
Frederick MD 21703
Web: scimedic.com
03-0096

Principal Display Panel – Tube Label

FAST REFIEF from everyday itch!

~Recommended By Women~

Vagi-cure

Anti-Itch Cream

Advanced Sensitive Medicated Cream

VAGI-CURE (REGULAR STRENGTH)
benzocaine, benzalkonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76466-075
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (BENZOCAINE)	BENZOCAINE	50 mg in 1 g
BENZALKONIUM CHLORIDE (BENZALKONIUM)	BENZALKONIUM CHLORIDE	.13 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
CETYL ALCOHOL
WATER
EDETATE DISODIUM
GLYCERYL MONOSTEARATE
ISOPROPYL MYRISTATE
ISOPROPYL PALMITATE
LANOLIN
METHYLPARABEN
MINERAL OIL
PEG-100 STEARATE
PROPYLENE GLYCOL
PROPYLPARABEN
.ALPHA.-TOCOPHEROL ACETATE

Packaging
#	Item Code	Package Description
1	NDC:76466-075-07	21 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	01/01/2011

Labeler - SCI International, Inc. DBA Continental Pharmaceuticals (114220648)

Establishment
Name	Address	ID/FEI	Operations
NATURAL ESSENTIALS, INC.		947484713	MANUFACTURE(76466-075)

Revised: 01/2018

Document Id: caa8ffd8-895a-46f9-8e89-2b408b336a9f

Set id: 2f685c77-86d2-4558-80e0-550846598e76

Version: 2

Effective Time: 20180124

SCI International, Inc. DBA Continental Pharmaceuticals

Further information

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

Medical Disclaimer