Label: CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid
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NDC Code(s):
70393-456-01,
70393-456-04,
70393-456-08,
70393-456-25, view more70393-456-80
- Packager: Future Diagnostics 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 August 27, 2020
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
- Uses
- Warnings
- Directions
- Storage
- Inactive ingredient
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SPL UNCLASSIFIED SECTION
Alcohol-Free Moisturizing Formula
Kills 99.99% of Germs*
Fragrance-Free & Hypoallergenic
Free of Triclosan, Parabens, Sulfates, Phthalates
*Kills 99.99% of common, harmful germs in just 15 seconds.
NDC 70393-456-25
ITEM# CTAFF10
NDC 70393-456-04
ITEM# CTAFF10-4
NDC 70393-456-01
ITEM# CTAFFS-T1
ITEM# FHS48
NDC# 70393-456-80
1800.758.3830
caretouchusa.com
Manufactured in China for Future Brands Brooklyn, NY 11220
- Packaging
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INGREDIENTS AND APPEARANCE
CARETOUCH ALCOHOL-FREE FOAMING HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70393-456 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BETAINE (UNII: 3SCV180C9W) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) PHENOXYETHANOL (UNII: HIE492ZZ3T) PALMITAMIDOPROPYLTRIMONIUM CHLORIDE (UNII: N2U96D202F) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70393-456-25 300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2019 2 NDC:70393-456-04 4 in 1 BAG 03/01/2019 2 NDC:70393-456-25 300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:70393-456-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2020 4 NDC:70393-456-08 8 in 1 PACKAGE 03/15/2020 4 NDC:70393-456-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:70393-456-80 48 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/01/2019 Labeler - Future Diagnostics Llc (080113296)