FDA.reportPublic FDA data

87708-002-04

Manufacturer
LEON UP GLOBAL HOLDING CORP | Chemco Corporation. | Chemco Corporation
Effective date
2026-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-16 05:10:08

Label at a glance#

ProductRENUEVO ANTI-DAMDRUFF
Active ingredientPYRITHIONE ZINC
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Pyrithione 2%

OTC - PURPOSE SECTION

Anti-Dandruff

INDICATIONS & USAGE SECTION

Helps prevent recurrence of flaking and itching associated with dandruff

WARNINGS SECTION

For external use only

Do not use on wounds or damaged skin or on a child under 12 years of age unless directed by a physician.

OTC - WHEN USING SECTION

Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Conditions worsens or does not improve after regular use of this product as directed

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help, or contact Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Wet hair. Shake well. Massage shampoo into scalp. Rinse. Repeat if desired.

For best results, use at least twice a week or as directed by a doctor.

For maximum dandruff control, use every time you shampoo.

OTHER SAFETY INFORMATION

See on the bottom of the bottle for lot number and expiration date.

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Acrylates Copolymer, Cocamide MEA, Cocamidopropylamine Oxide, Glycerin, Fragrance (Parfum), Polyquaternium-7, Sodium Hydroxide, Panthenol, Disodium EDTA, Citric Acid, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, Benzyl Salicylate, Butylphenyl Methylpropional, Citronellol, Geranyl Acetate, Hexyl Cinnamal, Linalool, Tetramethylacetyloctahydronaphthalenes.

OTC - QUESTIONS SECTION

Call 786 628 2540

RENUEVO ANTI DANDRUFF SHAMPOO

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTI DANDRUFFANTI DANDRUFF

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87708-00287708-002-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
SORBIC ACIDX045WJ989BIACT
EDETATE DISODIUM7FLD91C86KIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
CITRONELLOLP01OUT964KIACT
SALICYLIC ACIDO414PZ4LPZIACT
BENZYL ALCOHOLLKG8494WBHIACT
CITRIC ACID2968PHW8QPIACT
TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES2JU6ZH6GREIACT
GERANYL ACETATE3W81YG7P9RIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PANTHENOLWV9CM0O67ZIACT
WATER059QF0KO0RIACT
SODIUM HYDROXIDE55X04QC32IIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
LINALOOL, (+)-F4VNO44C09IACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
PYRITHIONE ZINCR953O2RHZ5ACTIB
COCAMIDE3YXD33R71GIACT
HEXYL CINNAMAL7X6O37OK2IIACT
BENZYL SALICYLATEWAO5MNK9TUIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RENUEVO ANTI-DAMDRUFFZINC PYRITHIONELEON UP GLOBAL HOLDING CORP5387b840-ad0a-4c20-e063-6294a90a59e32026-06-05WarningsExact identifier
ndc (package): 87708-002-04
ndc (product): 87708-002
ndc11 (package): 87708000204
spl id: 5387e88a-6050-ad77-e063-6294a90a8f78
spl set id: 5387b840-ad0a-4c20-e063-6294a90a59e3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.