Label: KEW HAND SANITISER SUMMER ROSE- alcohol spray
KEW HAND SANITISER PINEAPPLE AND PINK LOTUS- alcohol spray
KEW HAND SANITISER NARCISSUS LIME- alcohol spray
KEW HAND SANITISER GRAPEFRUIT AND LILY- alcohol spray
KEW HAND SANITISER BLUEBELL AND JASMINE- alcohol spray
KEW HAND SANITISER MAGNOLIA AND PEAR- alcohol spray
KEW HAND SANITISER FIG AND GRAPE- alcohol spray
KEW HAND SANITISER IRIS- alcohol spray
KEW HAND SANITISER MANGO- alcohol spray
KEW HAND SANITISER LAVENDER AND ROSEMARY- alcohol spray
KEW HAND SANITISER BERGAMOT AND GINGER- alcohol spray
KEW HAND SANITISER COCONUT- alcohol spray
KEW HAND SANITISER LEMONGRASS AND LIME- alcohol spray
KEW HAND SANITISER SANDALWOOD AND PINK PEPPER- alcohol spray
KEW HAND SANITISER ELDERFLOWER AND POMELO- alcohol spray
KEW HAND SANITISER OSMANTHUS ROSE- alcohol spray
KEW HAND SANITISER JASMINE PEACH- alcohol spray
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Contains inactivated NDC Code(s)
NDC Code(s): 81318-001-01, 81318-002-01, 81318-003-01, 81318-004-01, view more81318-005-01, 81318-006-01, 81318-007-01, 81318-008-01, 81318-009-01, 81318-010-01, 81318-011-01, 81318-012-01, 81318-013-01, 81318-014-01, 81318-015-01, 81318-016-01, 81318-017-01 - Packager: Christina May Ltd
- 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 January 4, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel NDC: 81318-001-01
- Package Label - Principal Display Panel NDC: 81318-002-01
- Package Label - Principal Display Panel NDC: 81318-003-01
- Package Label - Principal Display Panel NDC: 81318-004-01
- Package Label - Principal Display Panel NDC: 81318-005-01
- Package Label - Principal Display Panel NDC: 81318-006-01
- Package Label - Principal Display Panel NDC: 81318-007-01
- Package Label - Principal Display Panel NDC: 81318-008-01
- Package Label - Principal Display Panel NDC: 81318-009-01
- Package Label - Principal Display Panel NDC: 81318-010-01
- Package Label - Principal Display Panel NDC: 81318-011-01
- Package Label - Principal Display Panel NDC: 81318-012-01
- Package Label - Principal Display Panel NDC: 81318-013-01
- Package Label - Principal Display Panel NDC: 81318-014-01
- Package Label - Principal Display Panel NDC: 81318-015-01
- Package Label - Principal Display Panel NDC: 81318-016-01
- Package Label - Principal Display Panel NDC: 81318-017-01
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INGREDIENTS AND APPEARANCE
KEW HAND SANITISER SUMMER ROSE
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-002-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER PINEAPPLE AND PINK LOTUS
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-014-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER NARCISSUS LIME
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-015-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER GRAPEFRUIT AND LILY
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-003-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER BLUEBELL AND JASMINE
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-007-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER MAGNOLIA AND PEAR
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-009-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER FIG AND GRAPE
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-010-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER IRIS
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-011-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER MANGO
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-012-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER LAVENDER AND ROSEMARY
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-001-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER BERGAMOT AND GINGER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-008-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER COCONUT
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-013 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-013-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER LEMONGRASS AND LIME
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-004-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER SANDALWOOD AND PINK PEPPER
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-005-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER ELDERFLOWER AND POMELO
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-006-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER OSMANTHUS ROSE
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-016 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-016-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 KEW HAND SANITISER JASMINE PEACH
alcohol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81318-017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 78 mL in 78 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81318-017-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/04/2021 Labeler - Christina May Ltd (215632780) Registrant - Christina May Ltd (215632780) Establishment Name Address ID/FEI Business Operations Christina May Ltd 215632780 manufacture(81318-001, 81318-002, 81318-003, 81318-004, 81318-005, 81318-006, 81318-007, 81318-008, 81318-009, 81318-010, 81318-011, 81318-012, 81318-013, 81318-014, 81318-015, 81318-016, 81318-017)