ADVANCED HEALING- petrolatum ointment

Advanced Healing by

Drug Labeling and Warnings

Advanced Healing by is a Otc medication manufactured, distributed, or labeled by UNFI, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Petrolaturm 41%

Purpose

Skin protectant (ointment)

Uses

• temporarily protects minor: cuts, scrapes, burns
• temporarily protects and helps relieve chapped and cracked skin and lips
• helps protect from the drying effects of wind and cold weather

Warnings

For external use only

When using this product

• do not get in eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Do not use

• deep or puncture wounds
• animal bites
• serious burns

Keep out of reach of children

If swallowed get medical help or contract a Poison Control Center right away

Directions

• apply as needed

Inactive ingredients

minerol oil, ceresin, lanolin alcohol, panthenol, glycerin, bisabolol

SPL UNCLASSIFIED SECTION

This product is not manufactured or distributed by Beiersdorf Inc., owner of the registered trademark Aquaphor*

Distributed by Supervalu Inc., Eden Prairie, MN 55344 USA

247.000/247AB

Principal display panel

Equaline

Compare to Aquaphor Healing Oinment*

advanced

Healing Ointment

SKIN PROTECTANT

For dry cracked or iritated skin

Fragrance free

non-irritating

NET WT 2 OZ (56 g)

INGREDIENTS AND APPEARANCE

ADVANCED HEALING 
petrolatum ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-247
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	410 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
CERESIN (UNII: Q1LS2UJO3A)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
LEVOMENOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41163-247-41	396 g in 1 JAR; Type 0: Not a Combination Product	01/05/2009
2	NDC: 41163-247-07	9.9 g in 1 TUBE; Type 0: Not a Combination Product	01/05/2009
3	NDC: 41163-247-25	99 g in 1 JAR; Type 0: Not a Combination Product	01/05/2009
4	NDC: 41163-247-16	56 g in 1 TUBE; Type 0: Not a Combination Product	01/05/2009
5	NDC: 41163-247-06	198 g in 1 TUBE; Type 0: Not a Combination Product	01/05/2009

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/05/2009

Labeler - United Natural Foods, Inc. dba UNFI (943556183)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(41163-247)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(41163-247)