LOVALI LAVANDER SCENTED HAND SANITIZER 01- alcohol liquid LOVALI MINT SCENTED HAND SANITIZER 01- alcohol liquid LOVALI LEMON SCENTED HAND SANITIZER 01- alcohol liquid LOVALI ALEO VERA SCENTED HAND SANITIZER 01- alcohol liquid
Lovali Aleo Vera scented hand sanitizer by
Drug Labeling and Warnings
Lovali Aleo Vera scented hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang Meizhiyuan Cosmetics Co., Ltd, Townley Inc.. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- Hand Sanitizer
- Medicical Ingredient
- use
- WARNINGS
- Non-Medicinal
- Directions
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LOVALI LAVANDER SCENTED HAND SANITIZER 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 54304-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 64 mL in 100 mL Inactive Ingredients Ingredient Name Strength D&C VIOLET NO. 2 (UNII: 350KA7O6HK) 0.0002 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 100 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.5 mL in 100 mL TROLAMINE (UNII: 9O3K93S3TK) 0.3 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.05 mL in 100 mL CARBOMER 940 (UNII: 4Q93RCW27E) 0.3 mL in 100 mL FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) 0.2 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.05 mL in 100 mL WATER (UNII: 059QF0KO0R) 34.0998 mL in 100 mL Product Characteristics Color purple Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 54304-004-01 53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/03/2020 LOVALI MINT SCENTED HAND SANITIZER 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 54304-006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 64 mL in 100 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.00005 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 100 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.5 mL in 100 mL TROLAMINE (UNII: 9O3K93S3TK) 0.3 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.05 mL in 100 mL CARBOMER 940 (UNII: 4Q93RCW27E) 0.3 mL in 100 mL MINTLACTONE (UNII: X2T3I06CWR) 0.2 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.05 mL in 100 mL WATER (UNII: 059QF0KO0R) 34.09995 mL in 100 mL Product Characteristics Color yellow Score Shape Size Flavor LEMON Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 54304-006-01 53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/03/2020 LOVALI LEMON SCENTED HAND SANITIZER 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 54304-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 64 mL in 100 mL Inactive Ingredients Ingredient Name Strength FD&C YELLOW NO. 6 (UNII: H77VEI93A8) 0.00005 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 100 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.5 mL in 100 mL TROLAMINE (UNII: 9O3K93S3TK) 0.3 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.05 mL in 100 mL CARBOMER 940 (UNII: 4Q93RCW27E) 0.3 mL in 100 mL LEMON JUICE (UNII: AGN709ANTJ) 0.2 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.05 mL in 100 mL WATER (UNII: 059QF0KO0R) 34.0998 mL in 100 mL FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.00015 mL in 100 mL Product Characteristics Color yellow Score Shape Size Flavor LEMON Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 54304-003-01 53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/03/2020 LOVALI ALEO VERA SCENTED HAND SANITIZER 01
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 54304-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 64 mL in 100 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.00004 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 100 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.5 mL in 100 mL TROLAMINE (UNII: 9O3K93S3TK) 0.3 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.05 mL in 100 mL CARBOMER 940 (UNII: 4Q93RCW27E) 0.3 mL in 100 mL ALOE VERA FLOWER (UNII: 575DY8C1ER) 0.2 mL in 100 mL .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.05 mL in 100 mL WATER (UNII: 059QF0KO0R) 34.09988 mL in 100 mL FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.00008 mL in 100 mL Product Characteristics Color green Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 54304-005-01 53 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/03/2020 Labeler - Zhejiang Meizhiyuan Cosmetics Co., Ltd (543036597) Registrant - Townley Inc. (016956158) Establishment Name Address ID/FEI Business Operations Zhejiang Meizhiyuan Cosmetics Co., Ltd 543036597 manufacture(54304-003, 54304-004, 54304-005, 54304-006)
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.