y d b y e b v o d r e app issu ate d x i f u s · b o x app r o v e d b y d ate o p e r ator a r t...

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Page 1: y d b y e b v o d r e App Issu ate D x i f u S · B o x App r o v e d b y D ate O p e r ator A r t w o r k N submission C R N f i x R e a s o n e f S u f o r C ha n g Issu e d b y

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MHRA Header Box

Product Title

C Fonts Usedolours Used

Component

Pack Size

IG Code

Dimensions

Proof No. Date

Leaflet

25ml

25458202

297 x 200mm

2 14.12.2015

Process Black + 60%

Keyline (Does not print)

Fultium D3 Drops Internis

Helvetica

Rockwell

25458202

Page 2: y d b y e b v o d r e App Issu ate D x i f u S · B o x App r o v e d b y D ate O p e r ator A r t w o r k N submission C R N f i x R e a s o n e f S u f o r C ha n g Issu e d b y

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9

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tem

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MHRA Header Box

Product Title

C Fonts Usedolours Used

Component

Pack Size

IG Code

Dimensions

Proof No. Date

Leaflet

25ml

25458202

297 x 200mm

2 14.12.2015

Process Black + 60%

Keyline (Does not print)

Fultium D3 Drops Internis

Helvetica

Rockwell

This leaflet was last revised in 12/2015

Reporting of side effectsIf you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcardBy reporting side effects you can help provide more information on the safety of this medicine.

The Marketing Authorisation Holder is:Internis Pharmaceuticals Ltd.Linthwaite, Huddersfield, West YorkshireHD7 5QH, United KingdomThe Manufacturer is:UNIMEDIC ABBox 91, SE-864 21 MatforsSweden

25458202