Manufacturer record
VcarePharcos B11 & B12: regulatory record
Last checked 20 September 2026. Source: CDSCO monthly NSQ alerts and state drug-testing laboratories
2 batches manufactured by VcarePharcos B11 & B12 (Puducherry) were declared Not of Standard Quality between November 2024 and November 2024. Records are batch-specific findings by government laboratories as published in CDSCO's monthly alerts; where a company has stated that a flagged batch was counterfeit, that statement is noted when reported.
Records by type
2 records linked to VcarePharcos B11 & B12 in the datasets we hold. A zero means nothing is on record in those datasets, not that nothing ever happened. What the labels mean.
CDSCO drug alerts: Not of Standard Quality and spurious drugs
Scope. A company appearing here is not a finding that its products are unsafe. Regulatory actions can apply to one batch, one formulation, one period or one state. Always check the linked government document for the current position, and tell us if something is out of date. How we label records.
Flagged batches per year
All flagged batches
| Product | Batch | Reason declared NSQ | Tested by | Alert |
|---|---|---|---|---|
| Vcare Derma Essence Cosmetics | VCB018Mfg 2024-09 · Exp 2026-08 | NOT OF STANDARD QUALITY Content for Mercury found is more than 1ppm. But as per IS standards 16913:2018 the mercury content should not be more than 1 ppm, hence it is of Not of Standard Quality.Other | State Lab Drugs Control Laboratory, TelanganaState lab | Nov 2024 |
| Vcare Derma Essence | VCB019Mfg 2024-09 · Exp 2026-08 | NOT OF STANDARD QUALITY As per Rule 39 (Standareds of Cosmetics) Sub-Rule (5) Clause (b) of Cosmetics Rules, 2020, mercury in the finished cosmetic product shall not exceed one part per million (1 ppm) But the content for mercury found in the cream is more than 1 ppm. But as per IS 16913: 2018 the mercury content should not be more than 1 ppm, hence it is of Not of Standard Quality.Other | State Lab Drugs Control Laboratory, TelanganaState lab | Nov 2024 |
Right of reply. Manufacturers may submit a response or a laboratory re-test result; it is published unedited alongside this record. Submit a response.