OTC Medication Information: DR.SERSE Serum

DR.SERSE SERUM- glycerin gel
T.S international

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

GLYCERIN

Human Adipose Stromal Cell Conditioned Media, Water, 1,2-Hexanediol, Xanthan Gum, Cellulose, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyglyceryl-10 Laurate, Polyglyceryl-10 Myristate, Lactobacillus Ferment, Butylene Glycol, Ethylhexylglycerin, Allantoin, Algin, Tromethamine, Hydrogenated Lecithin, Sodium Acetate, Citric Acid, Menthol, Disodium EDTA, Polysorbate 60, Sorbitan Isostearate, Lactic Acid, Lavandula Angustifolia (Lavender) Oil, 3-O-Ethyl Ascorbic Acid, Hydroxyethylcellulose, Artemisia Capillaris Leaf Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Squalane, Sophora Angustifolia Root Extract, Collagen Extract, Copper Tripeptide-1, Acetyl Hexapeptide-8, rh-Polypeptide-1, rh-Oligopeptide-2, rh-Oligopeptide-1, Linalool

Skin protectant

keep out of reach of the children


1.Take out appropriate amount of this serum on the hand
2.spread it evenly on the skin.
3.Massage gently in the skin.
4.fully absorbs the product.


•Precautions when using

1. After using or using cosmetics, consult a specialist if you have any abnormal symptoms such as red spots, swelling or itching or side effects caused by direct sunlight.

2. Do not use on wounded area

3. storage and handling Precautions

a) Keep out of the reach of children

b) Store away from direct sunlight.

for external use only

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(click image for full-size original)

DR.SERSE SERUM
glycerin gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71540-0002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLYCERIN (GLYCERIN) GLYCERIN 1 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
HUMAN ADIPOSE
BUTYLENE GLYCOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71540-0002-1 5 TUBE, WITH APPLICATOR in 1 BOX contains a TUBE, WITH APPLICATOR
1 3.5 mL in 1 TUBE, WITH APPLICATOR This package is contained within the BOX (71540-0002-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part347 05/01/2017
Labeler — T.S international (689851767)
Registrant — T.S international (689851767)
Establishment
Name Address ID/FEI Operations
PICOSTECH Co.,Ltd. 557816754 manufacture (71540-0002)
Establishment
Name Address ID/FEI Operations
T.S INTERNATIONAL 689851767 label (71540-0002)

Revised: 06/2021 T.S international

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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