Label: HAND SANITIZER LIQUID WITH LAVENDER- isopropanol liquid
HAND SANITIZER LIQUID WITH LEMON- isopropanol liquid
NATURES FUSIONS DRAGONS BREATH HAND SANITIZER LIQUID- isopropanol liquid
UNSCENTED HAND SANITIZER LIQUID- isopropanol liquid
MINT/EUCALYPTUS/LEMON HAND SANITIZER LIQUID- isopropanol liquid
HAND SANITIZER LIQUID WITH IMMUNITY- isopropanol liquid
ANTIBAC ON THE GO- isopropanol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73769-000-30, 73769-001-01, 73769-001-02, 73769-001-04, view more73769-001-08, 73769-001-30, 73769-001-92, 73769-002-02, 73769-002-04, 73769-002-08, 73769-003-02, 73769-004-08, 73769-004-30, 73769-004-60, 73769-005-08, 73769-005-30, 73769-005-60, 73769-006-04, 73769-006-08 - Packager: NATURE'S FUSIONS, 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 April 12, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PURPOSE
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- WARNINGS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HAND SANITIZER LIQUID WITH LAVENDERÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  SODIUM PERCARBONATE (UNII: Z7G82NV92P)  LAVENDER OIL (UNII: ZBP1YXW0H8)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-004-30 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 2 NDC:73769-004-08 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/10/2020 3 NDC:73769-004-60 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2020 HAND SANITIZER LIQUID WITH LEMONÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  SODIUM PERCARBONATE (UNII: Z7G82NV92P)  LEMON OIL (UNII: I9GRO824LL)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-005-30 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 2 NDC:73769-005-08 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/10/2020 3 NDC:73769-005-60 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2020 NATURES FUSIONS DRAGONS BREATH HAND SANITIZER LIQUIDÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength CLOVE OIL (UNII: 578389D6D0)  EUCALYPTUS RADIATA LEAF OIL (UNII: SB9A7612BD)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  OREGANO LEAF OIL (UNII: 7D0CGR40U1)  PEPPERMINT OIL (UNII: AV092KU4JH)  CINNAMON BARK OIL (UNII: XE54U569EC)  LEMON OIL (UNII: I9GRO824LL)  SODIUM PERCARBONATE (UNII: Z7G82NV92P)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-001-30 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 03/16/2020 2 NDC:73769-001-02 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 3 NDC:73769-001-08 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 4 NDC:73769-001-04 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/27/2020 5 NDC:73769-001-92 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/29/2020 6 NDC:73769-001-01 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2020 UNSCENTED HAND SANITIZER LIQUIDÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  SODIUM PERCARBONATE (UNII: Z7G82NV92P)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-000-30 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2020 MINT/EUCALYPTUS/LEMON HAND SANITIZER LIQUIDÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength EUCALYPTUS OIL (UNII: 2R04ONI662)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)  LEMON OIL (UNII: I9GRO824LL)  SODIUM PERCARBONATE (UNII: Z7G82NV92P)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-002-02 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 2 NDC:73769-002-08 236.6 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/27/2020 3 NDC:73769-002-04 113 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2020 HAND SANITIZER LIQUID WITH IMMUNITYÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength CLOVE OIL (UNII: 578389D6D0)  EUCALYPTUS RADIATA LEAF OIL (UNII: SB9A7612BD)  ALOE VERA LEAF (UNII: ZY81Z83H0X)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  CINNAMON BARK OIL (UNII: XE54U569EC)  LEMON OIL (UNII: I9GRO824LL)  SODIUM PERCARBONATE (UNII: Z7G82NV92P)  ROSEMARY OIL (UNII: 8LGU7VM393)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-003-02 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/13/2020 ANTIBAC ON THE GOÂ
isopropanol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL  in 100 mL Inactive Ingredients Ingredient Name Strength THYME OIL (UNII: 2UK410MY6B)  ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  LEMON OIL (UNII: I9GRO824LL)  WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-006-08 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/26/2020 2 NDC:73769-006-04 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 08/26/2020 Labeler - NATURE'S FUSIONS, LLC (051472644) Establishment Name Address ID/FEI Business Operations NATURE'S FUSIONS, LLC 051472644 manufacture(73769-000, 73769-001, 73769-002, 73769-003, 73769-004, 73769-005, 73769-006)