View drug registration information details.
Items | Registration information |
ID | 572 |
No | 572 |
Brand Name | NEW V.ROHTO |
Ingredients | CHLORPHENIRAMINE 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 Form | OPHTHALMIC SOLUTION |
Primary Packaging | BOTTLE |
Storage | IN COOL PLACE, AWAY FROM DIRECT SUNLIGHT. |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 13 ML BOTTLE |
Dispensing Category | Prescription only |
ATC Classification | XX |
Pharmaceutical Class | ANTIPRURITUS |
Indications | EYESTRAIN, 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. |
Contraindications | PATIENTS WITH GLAUCOMA. |
Side Effects | NEW V.ROHTO CAN CAUSE ALLERGIES SUCH AS: EYE ITCHING, CONGESTION. STOP USING IT AND CONSULT WITH A PHYSICIAN OR PHARMACIST. |
Unit Price | - |
EDL |
No |
Description | CLEAR, COLORLESS TO PALE YELLOW SOLUTION |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | ROHTO - MENTHOLATUM ( VIETNAM) CO.,LTD |
Country | VIETNAM |
Import Registration No | VD -20092-13 |
Import Registration Date | 2013-11-08 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2023-02-27 |
FDD Registration No | 02 I 3823/13 |
FDD Registration Date | 2023-05-19 |
Expiry Date | 2026-05-18 |
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