Label: DR.PHI INSTANT HAND SANITIZER gel
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Contains inactivated NDC Code(s)
NDC Code(s): 58161-155-01, 58161-155-02, 58161-155-03 - Packager: MAMIBA
- 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 September 2, 2014
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- Official Label (Printer Friendly)
- Active Ingredient
- Drug Facts
- Purpose
- uses
- uses
- Warnings
- WHEN USING
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- other information
- inactive ingredients
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INGREDIENTS AND APPEARANCE
DR.PHI INSTANT HAND SANITIZER
dr.phi instant hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58161-155 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER 940 (UNII: 4Q93RCW27E) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58161-155-02 36 in 1 PACKAGE 1 NDC:58161-155-01 10 mL in 1 TUBE 2 NDC:58161-155-03 50 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/01/2014 Labeler - MAMIBA (558528988) Registrant - MAMIBA (558528988) Establishment Name Address ID/FEI Business Operations MAMIBA 558528988 manufacture(58161-155)