WEGMANS ORANGE SCENT- triclosan soap

Wegmans Orange Scent by

Drug Labeling and Warnings

Wegmans Orange Scent by is a Otc medication manufactured, distributed, or labeled by Sun Products Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Triclosan 0.10%

Use helps fight germs on hands when used as a hand soap

For external use only

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.  In case of eye contact, rinse thoroughly with water.

Directions wash hands and rinse

Antibacterial hand soap

Inactive ingredients  Water, Urea, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Alcohol Denat., Lauramine Oxide, Magnesium Chloride, Sodium Methyl 2-Sulfopalmitate, Fragrance, Sodium Metabisulfite, Disodium 2-Sulfopalmitate, Methyl Palmitate, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, FD&C Yellow No. 5, D&C Red No. 33

Questions? 1-800-Wegmans (934-6267) Ext 5920 9am-4pm EST workdays

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

WEGMANS ORANGE SCENT 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63691-026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
UREA (UNII: 8W8T17847W)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
ALCOHOL (UNII: 3K9958V90M)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)
METHYL PALMITATE (UNII: DPY8VCM98I)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63691-026-10	709 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/01/2014

Labeler - Sun Products Corporation (070931480)