Label: CLEAN TOUCH HAND SANITIZER- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73734-002-02, 73734-002-08, 73734-002-12, 73734-002-16, view more73734-002-17, 73734-002-24 - Packager: ViaClean Technologies, 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 November 25, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
Clean Touch
Hydrating hand sanitizer
Extended hand protection
Aloe Vera infused
Alcohol free/ fragrance free/ paraben and sulfate-free
Moisturizes using aloe vera and glycerin
Fast drying/instantly effective/ long-lasting protection
Non-flammable, non-staining, dye-free formula
Water-based formula is gentle on skin but tough on germs
Made in USA
(Manufactured and Distributed by)
ViaClean Technologies LLC
3939 Germantown Ave,Bldg. #2, Suite #2
Philadelphia, PA 19140
For additional product information: call 877-447-5956 or Visit www.bioprotect.us
(c) 2020 ViaClean Technologies All Rights Reserved
XXfl oz (XX mL) NDC 73734-002-XX
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INGREDIENTS AND APPEARANCE
CLEAN TOUCH HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73734-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4) WATER (UNII: 059QF0KO0R) ALOE (UNII: V5VD430YW9) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73734-002-16 473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/28/2020 2 NDC:73734-002-02 59.2 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/28/2020 3 NDC:73734-002-08 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/28/2020 4 NDC:73734-002-24 24 in 1 BOX 05/28/2020 4 NDC:73734-002-12 12 in 1 CARTON 4 NDC:73734-002-17 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/28/2020 Labeler - ViaClean Technologies, LLC (108814788) Registrant - ViaClean Technologies, LLC (108814788) Establishment Name Address ID/FEI Business Operations ViaClean Technologies, LLC 108814788 manufacture(73734-002) , label(73734-002) , pack(73734-002) , repack(73734-002) , relabel(73734-002) Establishment Name Address ID/FEI Business Operations Beauty Quest Group 117141741 manufacture(73734-002) , pack(73734-002) , label(73734-002) Establishment Name Address ID/FEI Business Operations Milbar Labs, Inc. 195556790 pack(73734-002) , label(73734-002)