Label: DR.TOC PERFECT CLEAN HAND WASH- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 70818-026-01 - Packager: C3 Co., Ltd.
- 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 14, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water
Disodium Cocoamphodiacetate
Glycerin
Sodium Chloride
Decyl Glucoside
Citric acid
Fragrance
Trehalose
Butylene Glycol
Hexylene glycol
Limonene
1,2-Hexanediol
Linalool
Hexyl Cinnamal
Sodium Hyaluronate
Portulaca Oleracea Extract
Ethylhexylglycerin
Coppertripeptide-1
Oligopeptide-14
Alanine
Arginine
Glycine
Glutamic Acid
Serine - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR.TOC PERFECT CLEAN HAND WASH
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70818-026 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.05 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70818-026-01 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/14/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 02/14/2021 Labeler - C3 Co., Ltd. (689846633) Registrant - C3 Co., Ltd. (689846633) Establishment Name Address ID/FEI Business Operations C3 Co., Ltd. 689846633 pack(70818-026) , manufacture(70818-026) , label(70818-026)
