FDA.reportPublic FDA data

Dr.eslee Triple Action BB

Manufacturer
Ajou Medics Co., Ltd
Effective date
2022-04-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:03:27

Label at a glance#

ProductDr.eslee Triple Action BB
Active ingredientADENOSINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

active ingredient: adenosine

INACTIVE INGREDIENT SECTION

inactive ingredient: Water, Butylene Glycol, Dipropylene Glycol, Cetyl Ethylhexanoate, Ethylhexyl Methoxycinnamate, Caprylic/Capric Triglyceride, Triethylhexanoin, Talc, Dimethicone, Phenyl Trimethicone, Isoamyl p-Methoxycinnamate, Arbutin, Cetyl PEG/PPG-10/1 Dimethicone, Zinc Oxide, Magnesium Sulfate, Polyglyceryl-4 Isostearate, Iron Oxides (CI 77492), Dipentaerythrityl Hexahydroxystearate / Hexastearate / Hexarosinate, Macadamia Integrifolia Seed Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Beeswax, Microcrystalline Wax, Disteardimonium Hectorite, Sorbitan Sesquioleate, Panthenol, Iron Oxides (CI 77499), Iron Oxides (CI 77491), Aluminum Hydroxide, Tocopheryl Acetate, Triethoxycaprylylsilane, Allantoin, Bisabolol, Farnesyl Acetate, Farnesol , Panthenyl Triacetate, PEG-8, Piper Methysticum Leaf/Root/Stem Extract, PEG-, /SMDI Copolymer, Aloe Barbadensis Leaf Juice, Portulaca Oleracea Extract, Chamaecyparis Obtusa Water, Hydrolyzed Collagen, Sodium Hyaluronate, Acetyl Hexapeptide-8, , Phenoxyethanol, Methylparaben, Propylparaben , Butylparaben, Fragrance

OTC - PURPOSE SECTION

Helps to protect from UV-Rays, skin whitening and wrinkle removing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Apply Proper Amount of the cream on skin.

WARNINGS SECTION

■ For external use only.
■ Avoid contact with eyes.
■ Do not swallow. If swallowed, get medical help.
■ Keep out of reach of children.
■ Stop use and ask doctor if rash and irritation develops.

DOSAGE & ADMINISTRATION SECTION

wash the skin to be applied

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label
package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76340-0006-12022-04-17C16284748780-1d6a99b39-9cd0-a426-e053-dadaa90af4c2Drug Facts
76340-0006-12022-01-28C16284748780-1d6a99b39-9cd0-a426-e053-dadaa90af4c2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76340-000676340-0006-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
DIPROPYLENE GLYCOLE107L85C40IACT
CETYL ETHYLHEXANOATE134647WMX4IACT
TRICAPRINO1PB8EU98MIACT
TRIETHYLHEXANOIN7K3W1BIU6KIACT
TALC7SEV7J4R1UIACT
DIMETHICONE92RU3N3Y1OIACT
ARBUTINC5INA23HXFIACT
ZINC OXIDESOI2LOH54ZIACT
MAGNESIUM SULFATE, UNSPECIFIEDDE08037SABIACT
FERRIC OXIDE RED1K09F3G675IACT
MACADAMIA OIL515610SU8CIACT
ADENOSINEK72T3FS567ACTIB

Source Document#

Source XML · Source PDF

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
dce5855e-d3cb-0518-e053-2a95a90a3ee867200a53-cbfd-62fc-e053-2991aa0a73552022-04-17WarningsExact identifier
spl id: dce5855e-d3cb-0518-e053-2a95a90a3ee8
spl set id: 67200a53-cbfd-62fc-e053-2991aa0a7355

Reported adverse events (FAERS/openFDA)#

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