VERADEX-E- petrolatum and lanolin ointment
ABBE Laboratories, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients
Petrolatum USP 58.95%
Anhydrous Lanolin USP 35%

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

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

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 from children.

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.

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

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

Product Label

VERADEX-E
petrolatum and lanolin ointment

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
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

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

#	Item Code	Package Description	Marketing Start Date
Packaging
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
5	NDC:68605-3700-6	400 g in 1 JAR; Type 0: Not a Combination Product	01/01/2008

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part347	01/01/2008

Labeler - ABBE Laboratories, Inc. (781745286)

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

Revised: 10/2022

Document Id: 5ea2c7e8-7869-4267-8bff-2e550ac01191

Set id: 00100102-c245-4b63-a4ff-794cacda6f17

Version: 5

Effective Time: 20221012

ABBE Laboratories, Inc.