UP AND UP ADVANCED SCAR- allantoin gel

Up and Up Advanced Scar by

Drug Labeling and Warnings

Up and Up Advanced Scar by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Allantoin,  0.5%

Purpose

Skin protectant 

Uses

• temporarily protects and helps relieve chapped or cracked skin

Warnings:

For external use only.

When using this product

• do not get into 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 on

• deep or puncture wounds, 
• animal bites, 
• serious burns.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply as needed

Other information

• store at room temperature.

Inactive ingredinets

water, PEG-200, alcohol denat., xanthan gum, phenoxyethanol, ethylhexylglycerin, allium cepa (onion) bulb extract, lecithin, panthenol (pro-vitamin B5), lactic acid, fragrance, hyaluronic acid, caramel, yellow 10.

Questions?

Call 1-800-910-6874

Package Labeling:

INGREDIENTS AND APPEARANCE

UP AND UP ADVANCED SCAR 
allantoin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYETHYLENE GLYCOL 9000 (UNII: V146K8QJ07)
ALCOHOL (UNII: 3K9958V90M)
XANTHAN GUM (UNII: TTV12P4NEE)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ONION (UNII: 492225Q21H)
DEXPANTHENOL (UNII: 1O6C93RI7Z)
LACTIC ACID (UNII: 33X04XA5AT)
HYALURONIC ACID (UNII: S270N0TRQY)
CARAMEL (UNII: T9D99G2B1R)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-700-20	1 in 1 BOX	08/01/2019
1		20 g in 1 TUBE; 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	08/01/2019

Labeler - Target Corporation (006961700)