Efficacy Study of Multiple Micro Nutrients Supplementation

Inclusion Criteria: * Apparently healthy Indonesian infants * Age 8-10 month at baseline visit * Willing to take 2 sachets of study product per day * Planning to reside in the study area during the next 14-16 months * Written informed consent by parent(s) or legally acceptable representative (in ICF there is statement that both are agree that child participate in the study) Exclusion Criteria: * Haemoglobin \< 8 g/dL at screening visit\*. * Significant congenital abnormality which according to investigator's clinical judgement will interfere the study conduct and assessment * Any known conditions likely to affect nutrient absorption diagnosed by the child's physician * Disorders requiring a special diet (such as food intolerance or food allergy or complaints such as reflux, constipation and cramps for which special formula is required). * Any other current or previous illnesses/conditions or intervention which according to investigator's clinical judgement could interfere the study conduct and assessment (e.g. chronic illness or physical or mental handicaps) * Regular use of MMN supplements syrup (every day in \> 1 week) within two weeks prior to entry into the study. * Not intending to use micronutrient supplements during the study * Participation in any other studies involving similar investigational or marketed products concomitantly or within two weeks prior to entry into the study. * Premature birth (gestational age \<37 weeks) * Low birth weight (\< 2500 g) * Severely under nutrition indicated by any of the following criteria: severely stunted: HAZ \< -3 SD; severely underweight WAZ \<-3 SD; wasted: WHZ \<-2 SD \*Subject with haemoglobin level (finger prick blood sample) at screening visit between 8-10 g/dL will be given iron syrup supplementation for 1 month. Thereafter, haemoglobin level (whole blood sample) will be checked at baseline visit: * If Hb \> 10 g/dL, subject is eligible for randomisation * If Hb \< 10 g/dL, subject is not eligible for randomisation and will be given iron syrup supplementation for 2 months