FDA.reportPublic FDA data

Up & Up Advanced Scar Gel

Manufacturer
Target Corporation
Effective date
2019-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:17:37

Label at a glance#

ProductUp and Up Advanced Scar
Active ingredientALLANTOIN
Label structure8 sections

Indications and uses

temporarily protects and helps relieve chapped or cracked skin

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Allantoin,  0.5%

Purpose

OTC - PURPOSE SECTION

Skin protectant 

Uses

INDICATIONS & USAGE SECTION

  • temporarily protects and helps relieve chapped or cracked skin

Warnings:

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Do not use on

OTC - DO NOT USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature.

Inactive ingredinets

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer PackageOuter PackageInner PackageInner Package

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-70011673-700-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYETHYLENE GLYCOL 9000V146K8QJ07IACT
ALCOHOL3K9958V90MIACT
XANTHAN GUMTTV12P4NEEIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ONION492225Q21HIACT
DEXPANTHENOL1O6C93RI7ZIACT
LACTIC ACID33X04XA5ATIACT
HYALURONIC ACIDS270N0TRQYIACT
CARAMELT9D99G2B1RIACT
D&C YELLOW NO. 1035SW5USQ3GIACT
ALLANTOIN344S277G0ZACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
fe25f85f-ef48-c4b4-e053-6294a90af9ef4d851934-aa91-4fe8-bb98-6fc2b78c45322023-06-15WarningsExact identifier
spl set id: 4d851934-aa91-4fe8-bb98-6fc2b78c4532

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.