Main label layout
Name and actives as one unit, dosage form, count and AUST L number placed and sized correctly, with the brand still leading.
Labels for vitamins, herbal and nutritional supplements that pass the TGA rules without looking like a prescription box. Including the move from TGO 92 to TGO 116.
Supplement label design is the design of the label and carton for a complementary medicine so it meets the TGA's labelling order and still sells: the main label, the regulatory panel, warnings, directions and every mandatory element laid out as part of the design.
It is the category where good designs most often fail on a technicality. The rules are precise, they belong to the TGA rather than the retailer, and they just changed. TGO 92 sunset on 1 October 2026. TGO 116 was published on 29 September 2026, and for five years a label may comply with either. From 1 October 2031 only TGO 116 applies.
Morice&Co. builds the regulatory content into the pack architecture from the brief, so the artwork clears compliance without a late redesign. The studio contributed to the Cenovis heritage rebuild, co-designed with Cowan Design, and writes the studio's own guide to supplement labelling in Australia.
The AUST L number, warnings, directions and permitted indications set the size of the panel before any design decision is made. Lock that block first and build the pack around its real size.
Listed medicine, assessed listed medicine or food. Get it wrong and the label is wrong from the first line. It is settled before design starts.
The TGA fixes what must be on the label, not how it looks. A well-designed regulatory panel is calmer and easier to read than a crowded one.
Every pack format has its own mandatory content and its own pinch points.
Name and actives as one unit, dosage form, count and AUST L number placed and sized correctly, with the brand still leading.
RASML and Permissible Ingredients Determination warnings in the exact wording, at the right size, in a layout people can actually read.
Existing labels reviewed and updated for TGO 116: microgram in full, warning prominence, distinguishing marks, 1.5 mm minimum text and large-capsule warnings.
Small bottles, sachets and blisters where the mandatory content will not fit on one panel, using cartons, peel-back and fold-out labels.
Protein, sports foods and fortified foods under the Food Standards Code, with a nutrition information panel and no therapeutic claims.
Artwork templates that keep every SKU compliant and consistent as the range grows.
For listed complementary medicines, these come from the TGA labelling order. They are fixed inputs to the design.
The product must be on the Australian Register of Therapeutic Goods. The AUST L number sits on the main label.
The medicine name with the active ingredients and their quantities, as one uninterrupted unit.
Only permitted ingredients, and claims drawn from the permitted indications. The claim hierarchy is designed around them.
Statements required by RASML, by the Permissible Ingredients Determination and by the Order, in the mandated wording.
Batch and expiry with prefixes, in a contrasting colour, and the sponsor's name and Australian address.
TGO 116 sets a clearer minimum text size of 1.5 mm. Panels are designed at real size and checked at print size.
Cenovis, co-designed with Cowan Design, and Natural Animal Solutions show regulatory content carried as design across a whole range.
An 88-year heritage vitamins brand codified into one brand book and packaging system for Chemist Warehouse, Priceline, Coles and Woolworths. Co-designed with Cowan Design.
Read the case studyGround-up rebrand of a vet-developed pet supplement brand sold through Petbarn, PetStock and Amazon. One system across identity, range architecture, packaging and retailer sales tools.
Read the case studyFixed fees, scoped to the brief. No hourly rates. A written proposal within five working days of a first conversation.
“Working with Morice was one of the best decisions we made. His creativity, strategic thinking, and attention to detail were exceptional. The result is a bold, modern brand identity that perfectly captures who we are.”
Adam Rumpf, CEO · Natural Animal Solutions
“The entire process is easy and enjoyable each time we work on a new project together. I'm consistently impressed with the speed, communication, eye for detail and quality of the finished product from Morice&Co.”
Kate Dawson, Marketing · Poseidon Animal Health
TGO 92, the TGA's labelling standard for non-prescription medicines, sunset on 1 October 2026. TGO 116 was published on 29 September 2026. For five years a label may comply with either, and from 1 October 2031 only TGO 116 applies. TGO 116 keeps the architecture of TGO 92 and tightens specific points, including a warning and actual-size image for large tablets and capsules, microgram written in full, more prominent warnings on listed medicines, a defined distinguishing mark for brand names and a clearer minimum text size of 1.5 mm.
The medicine name as one uninterrupted unit with the active ingredients and their quantities, the dosage form and quantity, and the AUST L number. The pack must also carry directions, warnings required by RASML and the Permissible Ingredients Determination, batch and expiry with prefixes, the sponsor's name and address, and excipient declarations where required.
Usually not. Most protein powders and sports nutrition products are foods under the Food Standards Code, often Standard 2.9.4, with a nutrition information panel and no therapeutic claims. Vitamins and herbal supplements with health indications are listed medicines under the TGA.
Yes. The studio reviews existing artwork against TGO 116, updates the regulatory panels and main labels, and plans the changeover so stock under TGO 92 and TGO 116 can co-exist during the transition. The sponsor remains responsible for regulatory sign-off.
Morice&Co. designs labels to the TGA labelling order and flags issues early, but is not a regulatory consultant. The sponsor is responsible for the listing, the indications and final regulatory sign-off, and complex products should be checked by a regulatory specialist.
Written proposal within five working days. Fixed fee, scoped to the brief. Response within two working days on every enquiry.
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