Label: HAND SANITIZER GIFT SET- alcohol kit
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Contains inactivated NDC Code(s)
NDC Code(s): 75997-027-01, 75997-028-01, 75997-029-01, 75997-030-01 - Packager: Papermates, Inc. DBA Noteworthy
- 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 July 6, 2011
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- STOP USE
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- STOP USE
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- STOP USE
- Keep out of reach of children.
- Directions
- Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER GIFT SET 3-PACK
alcohol kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75997-030 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75997-030-01 1 in 1 KIT Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 28 mL Part 2 1 BOTTLE 28 mL Part 3 1 BOTTLE 28 mL Part 1 of 3 GUM DROP HAND SANITIZER
ethyl alcohol liquidProduct Information Item Code (Source) NDC:75997-027 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) D&C RED NO. 33 (UNII: 9DBA0SBB0L) TROLAMINE (UNII: 9O3K93S3TK) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75997-027-01 28 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/28/2011 Part 2 of 3 PEPPERMINT HAND SANITIZER
ethyl alcohol liquidProduct Information Item Code (Source) NDC:75997-028 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75997-028-01 28 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/28/2011 Part 3 of 3 FROSTED BERRY HAND SANITIZER
ethyl alcohol liquidProduct Information Item Code (Source) NDC:75997-029 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE (UNII: V5VD430YW9) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) D&C RED NO. 33 (UNII: 9DBA0SBB0L) TROLAMINE (UNII: 9O3K93S3TK) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75997-029-01 28 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/28/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/06/2011 Labeler - Papermates, Inc. DBA Noteworthy (038734620)