Label: EMOJI ANTIBACTERIAL WIPES- benzalkonium chloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 70108-012-01 - Packager: Ashtel Studios, Inc.
- 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 February 12, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Use
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive Ingredients
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SPL UNCLASSIFIED SECTION
FRESH SCENT
ENRICHED WITH ALOE VERA
KILLS 99% OF GERMS
ANTIBACTERIAL
MOISTURIZING
STING-FREE
ECOFRIENDLY
ON THE GO PACK
Ultra Soft, Ultra Strong Antibacterial Sanitizing Wipes. Non-abrasive soft wipes won't scratch or dry out skin. Great alternative when soap and water are unavailable.
Smart Care®
WWW.SMARTCAREUS.COM ONTARIO, CA 91761
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1-877-274-8358 TOLL FREE IN US
1-909-434-0911 INTERNATIONALDESIGNED IN U.S.A.
MANUFACTURED IN CHINA
DISTRIBUTED BY ASHTEL STUDIOS INC.
- Packaging
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INGREDIENTS AND APPEARANCE
EMOJI ANTIBACTERIAL WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70108-012 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 g Inactive Ingredients Ingredient Name Strength BRONOPOL (UNII: 6PU1E16C9W) ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMOMILE (UNII: FGL3685T2X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) EDETATE SODIUM (UNII: MP1J8420LU) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70108-012-01 25 in 1 PACKET 02/08/2018 1 0.004 g 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 02/08/2018 Labeler - Ashtel Studios, Inc. (148689180)