Label: ZERNEL SCALP REJUVER ESSENCE- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 80152-302-01 - Packager: ZINOZEN CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 March 23, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Keep out of reach of children
- Stop use and ask a doctor if
- Do not use
- When using this product
- Directions
- Other information
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Inactive ingredients
Water, Glycerin, Alcohol, PEG-60 Hydrogenated Castor oil, Octyldodeceth-25, Betaine, l-Menthol, Caprylyl Glycol, Dexpanthenol, Disodium EDTA, Allantoin, Mentha Piperita (Peppermint) Oil, Glycine, Glutamic Acid, Lysine, Leucine, Alanine, Arginine, Isoleucine, Proline, Histidine, Cystine, Lavandula Angustifolia (Lavender) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Linalool, Lavandula Hybrida Oil,, Eucalyptus Globulus Leaf Oil, Amaranthus Hypochondriacus Seed Extract, Chenopodium Quinoa Extract
- Package Label
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INGREDIENTS AND APPEARANCE
ZERNEL SCALP REJUVER ESSENCE
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80152-302 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.1 mg in 100 mL Inactive Ingredients Ingredient Name Strength ALANINE (UNII: OF5P57N2ZX) ISOLEUCINE (UNII: 04Y7590D77) LAVENDER OIL (UNII: ZBP1YXW0H8) DEXPANTHENOL (UNII: 1O6C93RI7Z) AMARANTHUS HYPOCHONDRIACUS SEED (UNII: TWW80P29UN) PEPPERMINT OIL (UNII: AV092KU4JH) GLYCINE (UNII: TE7660XO1C) PROLINE (UNII: 9DLQ4CIU6V) HISTIDINE (UNII: 4QD397987E) CYSTINE (UNII: 48TCX9A1VT) LINALOOL, (+/-)- (UNII: D81QY6I88E) EUCALYPTUS OIL (UNII: 2R04ONI662) WATER (UNII: 059QF0KO0R) PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) OCTYLDODECETH-25 (UNII: F8934HEL3M) LEVOMENTHOL (UNII: BZ1R15MTK7) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ALLANTOIN (UNII: 344S277G0Z) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) BETAINE (UNII: 3SCV180C9W) CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X) GLUTAMIC ACID (UNII: 3KX376GY7L) LYSINE (UNII: K3Z4F929H6) LEUCINE (UNII: GMW67QNF9C) ARGININE (UNII: 94ZLA3W45F) ROSEMARY OIL (UNII: 8LGU7VM393) LAVANDIN OIL (UNII: 9RES347CKG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80152-302-01 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/07/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 05/07/2021 Labeler - ZINOZEN CO., LTD. (695580488) Registrant - ZINOZEN CO., LTD. (695580488) Establishment Name Address ID/FEI Business Operations ZINOZEN CO., LTD. 695580488 manufacture(80152-302)