Label: DERLADIE LABORATOIRE PORE TIGHTENING AMPOULE- niacinamide liquid
- NDC Code(s): 82083-0028-1
- Packager: LAON COMMERCE co ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 7, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Butylene Glycol
1,2-Hexanediol
Zinc PCA
Olea Europaea (Olive) Fruit Extract
Centella Asiatica Extract
Portulaca Oleracea Extract
Chamomilla Recutita (Matricaria) Flower Extract
Salvia Officinalis (Sage) Leaf Extract
Rosmarinus Officinalis (Rosemary) Leaf Extract
Salix Alba (Willow) Bark Extract
Melaleuca Alternifolia (Tea Tree) Extract
Tremella Fuciformis (Mushroom) Extract
Nelumbo Nucifera Flower Extract
Hamamelis Virginiana (Witch Hazel) Water
Glycerin
Sodium Hyaluronate
Caprylyl Glycol
Allantoin
Disodium EDTA
Ethylhexylglycerin - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
1. During using product or after use, if there are any
abnormal symptoms or side effects such as red spots,
swelling or itching in the area of use due to direct
sunlight, consult with a specialist.
2. Refrain from using on areas with scars, etc.
3. Precautions for storage and handling
A) Keep out of reach of chil
dren
B) Store away from direct sunlight
4.
Since a high dose of niacinamide is prescribed, please
adjust the amount after performing a skin sensitivity test
when using for the first time - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DERLADIE LABORATOIRE PORE TIGHTENING AMPOULE
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82083-0028 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 20 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CENTELLA ASIATICA (UNII: 7M867G6T1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82083-0028-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 12/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2023 Labeler - LAON COMMERCE co ltd (557839830) Registrant - LAON COMMERCE co ltd (557839830) Establishment Name Address ID/FEI Business Operations LAON COMMERCE CO Ltd 557839830 label(82083-0028) , manufacture(82083-0028)
