DERLADIE HERBALEXTRACT BODYSOLUTION MIST- niacinamide liquid 
LAON COMMERCE co ltd

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.

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Niacinamide

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

skin protect

KEEP OUT OF REACH OF THE CHILDREN

After showering, wipe off excess water and spray the product evenly 2-3 times on the desired area (except the face) at a distance of 15-20cm.

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

topical use only

1

DERLADIE HERBALEXTRACT BODYSOLUTION MIST 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82083-0023
Route of AdministrationVAGINAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE3 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN (UNII: 344S277G0Z)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
CENTELLA ASIATICA (UNII: 7M867G6T1U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82083-0023-1150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/2023
Labeler - LAON COMMERCE co ltd (557839830)
Registrant - LAON COMMERCE co ltd (557839830)
Establishment
NameAddressID/FEIBusiness Operations
LAON COMMERCE CO Ltd557839830manufacture(82083-0023) , label(82083-0023)

Revised: 7/2023
Document Id: 0185e220-a4a8-57b8-e063-6394a90a21aa
Set id: 0185e1ff-22a6-2daa-e063-6394a90a5d36
Version: 1
Effective Time: 20230728
 
LAON COMMERCE co ltd