Label: BE CLEAN- antibacterial hand soap liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 80590-002-01 - Packager: CLEANFORCE 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 October 14, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
DESCRIPTION
BE-CLEAN ANTIBACTERIAL HAND SOAP is an excellent multi purpose cleaner. Produces rich creamy lather for complete gentle cleansing action on grease, oil and other stubborn soils. Will not cause irritation or dryness, leaving the skin feeling soft and refreshed. It is an excellent replacement for powdered, liquid or bar soaps in high activity washrooms. May be dispensed in all types of liquid soap dispensers.
- DIRECTIONS:
- ACTIVE INGREDIENT
- CAUTION:
- KEEP OUT OF REACH OF CHILDREN
-
FIRST AID:
* EYES: In Case of contact, flush thoroughly with plenty of cool running water immediately. Remove contact lenses if worn. Continue flushing for 5-10 minutes holding eyelids apart. If irritation persists, get medical attention promptly.
* SKIN: When using this product discontinue use if irritation and redness developed. Stop use and ask to physician if skin irritation or redness occurs for more than 72 hours.
* INGESTION: If swallowed. do not induce vomiting. Drink plenty milk or water. Get Immediate medical aid.
- STATEMENT OF IDENTITY
-
Inactive Ingredients
Water 72.5%
Palmitic Acid 10%
Lauryl Ether Sulfate 4%
Myristic Acid 2.5%
Lauric Acid 2.5%
Glycol Distearate 2%
Potassium Chloride 1.25%
Glycerin 1.25%
Lauramidopropyl Betaine 1.25%
Sodium Lactate 0.8%
Coco Diethanolamide 0.8%
Phenoxyethanol (Preservative) 0.625%
Fragrance 0.375%
Sodium Benzoate 0.085%
Edetate Disodium 0.085%
- Purpose
- BE CLEAN ANTIBACTERIAL HAND SOAP
-
INGREDIENTS AND APPEARANCE
BE CLEAN
antibacterial hand soap liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80590-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength O-CYMEN-5-OL (UNII: H41B6Q1I9L) (O-CYMEN-5-OL - UNII:H41B6Q1I9L) O-CYMEN-5-OL 0.085 mg in 100 mg THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL 1.35 mg in 100 mg Inactive Ingredients Ingredient Name Strength SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM CHLORIDE (UNII: 660YQ98I10) WATER (UNII: 059QF0KO0R) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) COCO DIETHANOLAMIDE (UNII: 92005F972D) PALMITIC ACID (UNII: 2V16EO95H1) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCOL DISTEARATE (UNII: 13W7MDN21W) LAURIC ACID (UNII: 1160N9NU9U) 2-(2-(2-(2-PHENOXYETHOXY)ETHOXY)ETHOXY)ETHANOL (UNII: Y050HYR4XA) FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LACTATE (UNII: TU7HW0W0QT) MYRISTIC ACID (UNII: 0I3V7S25AW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80590-002-01 3972 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 10/12/2020 Labeler - CLEANFORCE LLC (012236173) Registrant - CLEANFORCE LLC (012236173) Establishment Name Address ID/FEI Business Operations CLEANFORCE LLC 012236173 manufacture(80590-002)
