Label: BQ PHARMA HAND SANITIZER- alcohol gel
BQ PHARMA HAND SANITIZER FRESH SCENT- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 78817-001-01, 78817-001-02, 78817-001-03, 78817-001-04, view more78817-001-05, 78817-001-06, 78817-002-03, 78817-002-04, 78817-002-05, 78817-002-06 - Packager: Frank por Laboratories, S.A. de C.V.
- Category: HUMAN OTC DRUG LABEL
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 August 25, 2020
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- Active Ingredient(s)
- Purpose
- Use(s)
- Warnings
- Directions
- Other Information
- Inactive Ingredients
- Questions or comments?
- Active Ingredient(s)
- Purpose
- Use(s)
- Warnings
- Directions
- Other Information
- Inactive Ingredients
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BQ PHARMA HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78817-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL .70 mL in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL (UNII: L7T10EIP3A) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78817-001-01 90 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/08/2020 2 NDC:78817-001-02 180 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/08/2020 3 NDC:78817-001-03 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 4 NDC:78817-001-04 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 5 NDC:78817-001-05 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 6 NDC:78817-001-06 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 06/08/2020 BQ PHARMA HAND SANITIZER FRESH SCENT
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:78817-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL .70 mL in 1 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL (UNII: L7T10EIP3A) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:78817-002-03 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 2 NDC:78817-002-04 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 3 NDC:78817-002-05 400 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 4 NDC:78817-002-06 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 09/15/2020 Labeler - Frank por Laboratories, S.A. de C.V. (812756987)
