Label: HAND SANITIZER FOAM- alcohol solution
- NDC Code(s): 77955-002-02
- Packager: Custom Chemical Solutions
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 22, 2024
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- Official Label (Printer Friendly)
- Active ingredients (v/v)
- Purpose
- Uses
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Warnings
For external use only: hands
Flammable. Keep away from fire or flame.
When using this productavoid contact with eyes.
In case of eye contact, flush eyes with water.
Avoid contact with broken skin.
Do not ingest or inhale.
- Directions:
- Other information:
- Inactive ingredients:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER FOAM
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77955-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) GLYCERIN (UNII: PDC6A3C0OX) BIS-PEG-10 DIMETHICONE/DIMER DILINOLEATE COPOLYMER (UNII: CF5W1YCX11) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77955-002-02 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/05/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 10/05/2020 Labeler - Custom Chemical Solutions (081096319) Establishment Name Address ID/FEI Business Operations Kutol Products Company 004236139 manufacture(77955-002)