VERADEX-E- petrolatum and lanolin ointment

VERADEX-E by

Drug Labeling and Warnings

VERADEX-E by is a Otc medication manufactured, distributed, or labeled by ABBE Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients
Petrolatum USP 58.95%
Anhydrous Lanolin USP 35%

PURPOSE

Purpose
Petrolatum USP 58.95%  ..................................  Protectant
Anhydrous Lanolin USP 35%  .......................  Protectant

INACTIVE INGREDIENT

Other ingredients: Tocopheryl Acetate, Cetyl Esters, Ethyl Methylphenylglycidate, Benzyl Cinnamate, Salicylic Acid.

WARNINGS

Warnings: For external use only.
Discontinue use if signs of irritation appear. If condition worsens consult a doctor.
Do not use over deep, infected, or puncture wounds.

KEEP OUT OF REACH OF CHILDREN

Keep from children.

INDICATIONS & USAGE

Indications: Temporarily relieves minor burns, dry, chapped, fissured and macerated skin and lips, also relieves Psoriais, Eczema, mild sunburn, abrasions and contusions, diaper dermatitis, hemorrhoids, and prickly heat.

DOSAGE & ADMINISTRATION

Directions: Apply a thin film to clean, dry skin three times daily. May be covered with sterile gauze, if desired.

PRINCIPAL DISPLAY PANEL

NDC: 68605-3700-5

VERADEX-E® OINTMENT

Super Emollient, Protectant
Healing Ointment

Net Wt. 100g.

U.S. Pat. # 5,645,826

ABBE LABORATORIES, INC.TM
Farmingdale, NY 11735

INGREDIENTS AND APPEARANCE

VERADEX-E 
petrolatum and lanolin ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68605-3700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	589.5 mg  in 1 g
LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H)	LANOLIN	350 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CETYL ESTERS WAX (UNII: D072FFP9GU)
ETHYL METHYLPHENYLGLYCIDATE (UNII: UD51D5KR4A)
BENZYL CINNAMATE (UNII: V67O3RO97U)
SALICYLIC ACID (UNII: O414PZ4LPZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68605-3700-2	15 g in 1 JAR; Type 0: Not a Combination Product	01/01/2008
2	NDC: 68605-3700-3	28 g in 1 JAR; Type 0: Not a Combination Product	01/01/2008
3	NDC: 68605-3700-4	56 g in 1 JAR; Type 0: Not a Combination Product	01/01/2008
4	NDC: 68605-3700-5	100 g in 1 JAR; Type 0: Not a Combination Product	01/01/2008	10/31/2023
5	NDC: 68605-3700-6	400 g in 1 JAR; Type 0: Not a Combination Product	01/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/01/2008

Labeler - ABBE Laboratories, Inc. (781745286)

Establishment
Name	Address	ID/FEI	Business Operations
ABBE Laboratories, Inc.		781745286	manufacture(68605-3700)