Label: PURTOUCH ANTISEPTIC WET WIPES- ethyl alcohol cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 79581-601-60 - Packager: Purtouch 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 July 31, 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
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Warnings
Flammable, keep away from fire/flame
For external use only
Do not use
• in children less than 2 months of age
• on open skin wounds
• if you are allergic to any of the ingredients
When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if
• irritation and redness develop
• condition persists for more than 72 hours
- Directions
- Other information
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SPL UNCLASSIFIED SECTION
TRUSTED BY PROFESSIONALS
70% ALCOHOL
Peace of Mind with PurTouch
PurTouch is here to give you and your loved ones comfort in knowing that whatever life throws in front of you, you can walk away clean. Our commercial sanitizing wipes helps to reduce bacteria with Aloe and Vitamin E it’s gentle on your hands.
PurTouch Gives Back
PurTouch is committed to keeping everyone safe and clean. We pledge to donate a portion of proceeds, through providing free hand sanitizer and wipes to organizations in need. Thank you for helping us support these important causes!
HANDS
PLEASE RECYCLE
Intended For External Use Only
Lot No:
Expiry:
Distributed by:
PurTouch LLC, 343 Soquel Ave #190, Santa Cruz, CA, 95062COUNTRY OF ORIGIN: CHINA
info@purtouchclean.com
- Packaging
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INGREDIENTS AND APPEARANCE
PURTOUCH ANTISEPTIC WET WIPES
ethyl alcohol clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79581-601 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BETAINE (UNII: 3SCV180C9W) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) CETYLPYRIDINIUM CHLORIDE ANHYDROUS (UNII: 6BR7T22E2S) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) PROPANEDIOL (UNII: 5965N8W85T) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79581-601-60 60 in 1 CANISTER 07/18/2020 1 4.584 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 not final part333A 07/18/2020 Labeler - Purtouch Llc (117574172)
