Label: SCRUBS FOAMING HAND SANITIZER SCRUBS- hand sanitizer foam solution
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Contains inactivated NDC Code(s)
NDC Code(s): 51239-1929-7 - Packager: ITW Dymon
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated October 21, 2009
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INGREDIENTS AND APPEARANCE
SCRUBS FOAMING HAND SANITIZER SCRUBS
hand sanitizer foam solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51239-1929 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.1 g in 970 mL BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 970 mL Inactive Ingredients Ingredient Name Strength Mineral Oil (UNII: T5L8T28FGP) 0.7 g in 970 mL Isopropyl Myristate (UNII: 0RE8K4LNJS) 0.3 g in 970 mL Alcohol (UNII: 3K9958V90M) 20 g in 970 mL Water (UNII: 059QF0KO0R) 78.02 g in 970 mL Product Characteristics Color Score Shape Size Flavor LEMON Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51239-1929-7 252 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 10/01/2009 Labeler - ITW Dymon (103307604) Registrant - ITW Dymon (103307604) Establishment Name Address ID/FEI Business Operations ITW Dymon 103307604 manufacture