Label: DERLADIE HERBALEXTRACT BODYSOLUTION MIST- niacinamide liquid
- NDC Code(s): 82083-0023-1
- Packager: LAON COMMERCE co ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated July 28, 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
Glycolic Acid
Butylene Glycol
1,2-Hexanediol
Betaine Salicylate
Salicylic Acid
Alpha-Arbutin
Dipropylene Glycol
Menthol
Glutathione
Betaine
Allantoin
Camellia Sinensis Leaf Extract
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
Glycerin
Melaleuca Alternifolia (Tea Tree) Leaf Oil
Alcohol Denat.
PEG-60 Hydrogenated Castor Oil
Sodium Hyaluronate
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 children
B) Store away from direct sunlight
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DERLADIE HERBALEXTRACT BODYSOLUTION MIST
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82083-0023 Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 3 g in 100 mL Inactive Ingredients Ingredient Name Strength ALLANTOIN (UNII: 344S277G0Z) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CENTELLA ASIATICA (UNII: 7M867G6T1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82083-0023-1 150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2023 Labeler - LAON COMMERCE co ltd (557839830) Registrant - LAON COMMERCE co ltd (557839830) Establishment Name Address ID/FEI Business Operations LAON COMMERCE CO Ltd 557839830 manufacture(82083-0023) , label(82083-0023)
