View drug registration information details.


ItemsRegistration information
ID572
No572
Brand NameNEW V.ROHTO
IngredientsCHLORPHENIRAMINE MALEATE 1.30 MG, DIPOTASSIUM GLYCYRRHIZAINATE 13 MG, PANTHENOL 13 MG, VITAMIN B6 6.50 MG, POTASSIUM L-ASPARTATE 130 MG, SODIUM CHONDROITIN SULFATE 13 MG, TETRAHYDROZOLINE HYDROCHLORIDE 1.30 MG/13 ML
Dosage FormOPHTHALMIC SOLUTION
Primary PackagingBOTTLE
StorageIN COOL PLACE, AWAY FROM DIRECT SUNLIGHT.
Shelf Life3 YEARS
Pack SizeBOX OF 13 ML BOTTLE
Dispensing CategoryPrescription only
ATC ClassificationXX
Pharmaceutical ClassANTIPRURITUS
IndicationsEYESTRAIN, CONJUNCTIVAL CONGESTION, OPHTHALMIA DUE TO UV AND OTHER LIGHT RAYS,EYE ITCHING, BLEPHARITIS, BLURRED VISION, DISCOMFORT DUE TO THE USE OF HARD CONTACT LENSES, EYE MOISTURIZATION.
ContraindicationsPATIENTS WITH GLAUCOMA.
Side EffectsNEW V.ROHTO CAN CAUSE ALLERGIES SUCH AS: EYE ITCHING, CONGESTION. STOP USING IT AND CONSULT WITH A PHYSICIAN OR PHARMACIST.
Unit Price-
EDL No
DescriptionCLEAR, COLORLESS TO PALE YELLOW SOLUTION
Note
License OwnerDKSH LAOS COMPANY LIMITED
ManufacturerROHTO - MENTHOLATUM ( VIETNAM) CO.,LTD
CountryVIETNAM
Import Registration NoVD -20092-13
Import Registration Date2013-11-08
ActivityCERTIFICATE RELEASED
Applied Date2023-02-27
FDD Registration No02 I 3823/13
FDD Registration Date2023-05-19
Expiry Date2026-05-18

Back to drug list