Label: PARALAPIEL CLINIC SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 77499-0001-1 - Packager: Charming Cosmetics. 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 May 13, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Glycerin, Honey extract, Carthamus tinctorius (Safflower) flower extract, Rosa damascena flower extract, Chrysanthemum indicum flower extract, Calendula officinalis flower extract, Oenothera biennis (Evening primrose) flower extract, Nelumbo nucifera flower extract, Lavandula angustifolia (Lavender) flower extract, Inula britannica flower extract, Lonicera japonica (Honeysuckle) flower extract, Aloe barbadensis leaf juice, Sodium hyaluronate, Potassium hydroxide, Carbomer, Butylene glycol, Fragrance
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
For external use only. Flammable, Keep away from fire or flames.
Do not use■ in children less than 2 months of age
■ on open skin wounds
when using this product keep out of eyes, ears, and mouth.
Stop use and ask a doctor if irritation or rash occurs. these may be signs of a serious condition.
Keep out of reach of children. if swallowed, get medical help or contact a poison control center right away. - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PARALAPIEL CLINIC SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77499-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 37.2 mL in 60 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) ALOE (UNII: V5VD430YW9) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) HYALURONIC ACID (UNII: S270N0TRQY) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77499-0001-1 60 mL in 1 TUBE; Type 0: Not a Combination Product 05/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/01/2020 Labeler - Charming Cosmetics. Co. Ltd (689935740) Registrant - Charming Cosmetics. Co. Ltd (689935740) Establishment Name Address ID/FEI Business Operations Charming Cosmetics. Co. Ltd 689935740 manufacture(77499-0001)