FDA.reportPublic FDA data

Pelo Baum Lash Lash

Manufacturer
Caregen Co.,Ltd.
Effective date
2021-09-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:36:01

Label at a glance#

ProductPelo Baum Lash Lash
Active ingredientAllantoin
Label structure8 sections

Indications and uses

Eyelash enhancer enriched with peptide complex, Helps to improve the appearance of natural lash length, fullness and thickness.

Dosage and administration

Apply a thin line of Pelo Baum Lash Lash to your cleansed upper lash line once a day at night, as though you were applying liquid eyeliner, leave it at least for 4 hours.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua), Phenoxyethanol, Sodium Hyaluronate, Hydroxypropyl Methylcellulose, Glycerin, Arginine, Glycine Soja (Soybean) Oil, Disodium EDTA, Citric Acid, Hydrogenated Lecithin, Decapeptide-10, Oligopeptide-54, Decapeptide-18, Acetyl Decapeptide-3, Oligopeptide-42, Sodium Oleate, Biotin

PURPOSE

OTC - PURPOSE SECTION

Skin Protectant

WARNINGS

WARNINGS SECTION

For external use only, do not swallow. In case of accidental ingestion, seek medical assistance. Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and consult a doctor if rash or irritation occurs. Do not apply directly to a wound or open cut. Keep out of reach of children. Store at room temperature (below 25℃).

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

Eyelash enhancer enriched with peptide complex, Helps to improve the appearance of natural lash length, fullness and thickness.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a thin line of Pelo Baum Lash Lash to your cleansed upper lash line once a day at night, as though you were applying liquid eyeliner, leave it at least for 4 hours.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60716-090-022021-09-16C16284748780-19d75b9d0-8ca1-f424-e053-dadaa90a57cede747df7-8eab-4910-9ca2-98f764f568e4
60716-090-022020-01-31C16284748780-19d75b9d0-8ca1-f424-e053-dadaa90a57cede747df7-8eab-4910-9ca2-98f764f568e4

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60716-09060716-090-01, 60716-090-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Allantoin344S277G0ZACTIB
Water059QF0KO0RIACT
PhenoxyethanolHIE492ZZ3TIACT

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
0103f90d-093e-4e83-8805-026f43111f83de747df7-8eab-4910-9ca2-98f764f568e42023-12-11WarningsExact identifier
spl set id: de747df7-8eab-4910-9ca2-98f764f568e4

Reported adverse events (FAERS/openFDA)#

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