ADVANCED RELIEF A AND D- petrolatum ointment

Advanced Relief A and D by

Drug Labeling and Warnings

Advanced Relief A and D by is a Otc medication manufactured, distributed, or labeled by Ultra Seal Corporation, ULTRAtab Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient (in each gram): White Petrolatum 93.5%

PURPOSE

Purpose-Skin Protectant

INDICATIONS & USAGE

Uses-Temporarily protects minor cuts, scrapes, and burns.  Temporarily protects and helps chapped or cracked skin and lips.  Helps protect lips from drying effects of wind and cold weather.

DOSAGE & ADMINISTRATION

Directions: Apply as needed

KEEP OUT OF REACH OF CHILDREN

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

WARNINGS

For external use only.  Do not use in eyes, on deep puncture wounds, animal bites, or serious burns or for more than 1 week unless directed by a doctor.

Stop use and ask a doctor if: A rash or allergic reaction develops.  Condition worsens, persists, or recurs.

INACTIVE INGREDIENT

Inactive Ingredients: Corn Oil, Light Mineral Oil, Vitamin A Palmitate, Vitamin D

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ADVANCED RELIEF A AND D 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42213-375
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	937.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
CORN OIL (UNII: 8470G57WFM)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ERGOCALCIFEROL (UNII: VS041H42XC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42213-375-47	144 in 1 CARTON	12/01/2011
1	NDC: 42213-375-05	5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	12/01/2011

Labeler - Ultra Seal Corporation (085752004)

Registrant - ULTRAtab Laboratories, Inc. (151051757)

Establishment
Name	Address	ID/FEI	Business Operations
Ultraseal Corporation		085752004	pack(42213-375)

Establishment
Name	Address	ID/FEI	Business Operations
Ultratab Laboratories, Inc.		151051757	manufacture(42213-375)