Label: FOMIN MINI HAND SANITIZER WIPES - 6 - VARIETY PACK- benzalkonium chloride kit
- NDC Code(s): 85755-004-06
- Packager: Fomin LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated July 3, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient:
- Purpose:
- Use:
- Warnings:
- Directions:
- Inactive Ingredients:
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SPL UNCLASSIFIED SECTION
KILLS 99.9% OF GERMS
ALCOHOL FREE FORMULA
Clean Hands, Wherever You Go
HYALURONIC ACID
ALOE VERA
Packed With Fresh Scents
2 X MELON POP
2 X COCO-NILLA BLISS
2X FRAGRANCE FREE
Clean For You & Our Planet
Stay fresh and protected wherever you go with Fomin Hand Sanitizer Wipes. Designed for effective cleansing, these wipes eliminate 99.9% of germs and bacteria while keeping your hands soft and nourished. Unlike harsh sanitizers, our gentle, alcohol-free formula won't dry out your skin, making them ideal for all skin types.
99.9% GERM PROTECTION
HYPOALLERGENIC
DERMATOLOGIST-TESTED & BABY-SAFE
When You Need It The Most
GYM KIDS
PURSE TRAVELSafe for Children
DISCLAIMER: For external use only (including intimate areas). Avoid contact with eyes; if contact occurs, rinse thoroughly with water. Do not apply to broken or irritated skin. Discontinue use if irritation or redness appears. Keep out of reach of children. Do not flush wipes down the toilet - dispose responsibly. STORAGE: Store in a cool, dry place. Keep sachets sealed until use.
QUESTIONS: For questions and general information visit us at fominsoap.com/contact@fominsoap fominsoap.com
Manufactured for Petra Brands Co., Limited.
Distributed by Fomin LLC, Wilmington, DE 19801, USA.
Designed in USA. Made in PRC
www.fominsoap.com1% FOR THE PLANET
LEAPING BUNNY CERTIFIED
PLASTIC BANK CERTIFIED
OEKO-TEX® CERTIFIED ORGANIC COTTON
HYDRATING
Plant-Based Wipes
- Packaging
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INGREDIENTS AND APPEARANCE
FOMIN MINI HAND SANITIZER WIPES - 6 - VARIETY PACK
benzalkonium chloride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85755-004 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85755-004-06 1 in 1 BOX 06/20/2025 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 16 PACKAGE 0.056 mL Part 2 16 PACKAGE 0.056 mL Part 3 16 PACKAGE 0.056 mL Part 1 of 3 FOMIN MINI HAND SANITIZER WIPES COCO-NILLA BLISS
benzalkonium chloride clothProduct Information Item Code (Source) NDC:85755-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB) CHAMOMILE (UNII: FGL3685T2X) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 8 in 1 PACKET 1 0.0035 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 06/20/2025 Part 2 of 3 FOMIN MINI HAND SANITIZER WIPES MELON POP
benzalkonium chloride clothProduct Information Item Code (Source) NDC:85755-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB) CHAMOMILE (UNII: FGL3685T2X) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 8 in 1 PACKET 1 0.0035 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 06/20/2025 Part 3 of 3 FOMIN MINI HAND SANITIZER WIPES FRAGRANCE FREE
benzalkonium chloride clothProduct Information Item Code (Source) NDC:85755-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PHENOXYETHANOL (UNII: HIE492ZZ3T) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB) CHAMOMILE (UNII: FGL3685T2X) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 8 in 1 PACKET 1 0.0035 mL in 1 PACKAGE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 06/20/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/20/2025 Labeler - Fomin LLC (118983680)

