SHOP RITE ULTRA SO-SOFT- triclosan soap

Shop Rite Ultra So-soft by

Drug Labeling and Warnings

Shop Rite Ultra So-soft by is a Otc medication manufactured, distributed, or labeled by Sun Products Corporation, Wakefern, Sun Products Corporation - Salt Lake City, Sun Products Corporation - Bowling Green. 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, TEA-Dodecylbenzenesulfonate, Sodium Laureth Sulfate, Sodium Methyl 2-Sulfopalmitate, Lauramine Oxide, Sodium Lauryl Sulfate, Alcohol Denat., Disodium 2-Sulfopalmitate, Methyl Palmitate, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, Yellow No. 5, Red No. 33

Questions? 1-888-723-3929

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

SHOP RITE ULTRA SO-SOFT 
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63691-021
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)
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALCOHOL (UNII: 3K9958V90M)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
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: 63691-021-10	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)

Registrant - Wakefern (006972418)

Establishment
Name	Address	ID/FEI	Business Operations
Sun Products Corporation - Salt Lake City		096752865	manufacture(63691-021)

Establishment
Name	Address	ID/FEI	Business Operations
Sun Products Corporation - Bowling Green		809709314	manufacture(63691-021)