REEVA ANTIBACTERIAL GREEN APPLE- triclosan soap
Sun Products Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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, Sodium Lauryl Sulfate, Sodium Laureth Sulfate, Lauramine Oxide, Sodium Dodecylbenzenesulfonate, Sodium Xylene Sulfonate, Alcohol Denat., Fragrance, Sodium Citrate, Methylchloroisothiazolinone, Methylisothiazolinone, Benzophenone-4, Blue No. 1, Yellow No. 5

front label

LBLFR

back label

LBLBK

REEVA ANTIBACTERIAL GREEN APPLE
triclosan soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63691-020
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALCOHOL (UNII: 3K9958V90M)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63691-020-10	709 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2014

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

Labeler - Sun Products Corporation (070931480)