Label: BLUZEN - WINTER PINE, WINTERMINT, PEPPERMINT - KIT- ethyl alcohol kit
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Contains inactivated NDC Code(s)
NDC Code(s): 79200-605-02, 79200-606-02, 79200-607-16, 79200-705-02 - Packager: Remcoda, Llc
- 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 11, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- BLUZEN HAND SANITIZER WINTER PINE
- Active ingredient
- Purpose
- INDICATIONS & USAGE
- Warnings
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- BLUZEN HAND SANITIZER PEPPERMINT
- Active ingredient
- Purpose
- INDICATIONS & USAGE
- Warnings
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- BLUZEN HAND SANITIZER WINTERMINT
- Active ingredient
- Purpose
- INDICATIONS & USAGE
- Warnings
- Directions
- Other information
- Inactive ingredients
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- KIT LABEL
- KIT COMPONENTS LABEL
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INGREDIENTS AND APPEARANCE
BLUZEN - WINTER PINE, WINTERMINT, PEPPERMINT - KIT
ethyl alcohol kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79200-705 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79200-705-02 1 in 1 KIT; Type 0: Not a Combination Product 09/11/2020 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE, PUMP 60 mL Part 2 1 BOTTLE, PUMP 60 mL Part 3 1 BOTTLE, PUMP 60 mL Part 1 of 3 BLUZEN HAND SANITIZER WINTER PINE
ethyl alcohol liquidProduct Information Item Code (Source) NDC:79200-605 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 WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79200-605-02 60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/11/2020 Part 2 of 3 BLUZEN HAND SANITIZER PEPPERMINT
ethyl alcohol liquidProduct Information Item Code (Source) NDC:79200-606 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 WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79200-606-02 60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/11/2020 Part 3 of 3 BLUZEN HAND SANITIZER WINTERMINT
ethyl alcohol liquidProduct Information Item Code (Source) NDC:79200-607 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 WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79200-607-16 60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/11/2020 Labeler - Remcoda, Llc (117130169)