Private Label

Private Labelling is an excellent 'beat the competition tool'.

Private Labelling puts you in control of your profit margins and marketing of your products

To produce your own labels is a very expensive business, minimum quantities are usually very high. For many retailers private labelling was out of reach.

American Dietary Laboratories entered the private label business in the 1970's, establishing the finest private label program available, not the biggest …just the best.

This unique program offers more possibilities to the small, medium or large retailer planning to enter the market with a minimum cash outlay. The program allows the retailer to have greater cash flow, with less cash tied up in inventory and fresher stock on the shelves.

This program will provide you with one of the most complete lines of dietary supplements available from any vitamin company in the world.

High quality NNFA Trulabel program
Full product disclosure
Certificate of analysis on all the products
Customer approved labels
UPC coded
Lot number coded by manufacturer batches
"Best before" date for guaranteed freshness
Full "body seal" protection
High service level "in stock history
Re-order shipments processed within 24 hours
Minimum order for each product first time 6 boxes of 12 bottles each, minimum re-order 3 boxes of 12 bottles.

Step1: Create your own Logo and information (company address etc)

Step2: Provide us your Logo on 300 DPI resolutions, TIFF, or EPS files,

Step3: Chose the colours for your label

Step 4: P.s: if you don't have a logo we will help design one for you at a nominal fee

American Dietary Laboratories will pay for all the printing costs but if you want more complicated graphics and colours it may require the use of an outside printer which will increase your costs.

The ADL group use only the most natural ingredients, or as close as possible to those found in nature, as the basic compounding in food supplements.

All mixing, blending, tableting, encapsulation and packaging are performed with stainless steel equipment according to good manufacturing practices.

After meeting quarantine and analysis procedures, the required amount of basic raw materials are carefully measured and verified. They are then mixed in stainless steel blenders where sweetening and flavouring agents (if required by the formulation) are added.

After being thoroughly mixed, they are drawn off into sterile drums to be transported to the tableting or encapsulation areas as appropriate.

All tableting and encapsulation is done in special isolated places where only one product at the time can be made to prevent cross contamination of ingredients.

The blended ingredients are placed in a stainless steel hopper which feeds directly into the tableting press, the proper amount of mix is fed into each die (or capsule) and the proper pressure applied to create the tablet. The tablet is then fed directly into a special lined container for transport to the next production process.

The product is then taken to the coating room if applicable where the tablets are spray- coated with a natural material in stainless steel revolving drums. It should be noted that in the blending, tableting and coating processes, no chemical, moisture or heat are applied to our food supplements.

All the personnel involved in each stage of manufacture or packaging are completely dressed in clean uniforms, properly hatted and gloved.

A 100% visual inspection of all powders and tablets is made at the completion of blending, tableting, coating and packaging.

Any broken or defective tablets are removed and rejected by the inspection personnel.

Samples of all the tablets and capsules are inspected after manufacture in laboratories by our Quality control personnel in accordance with good manufacturing practices as designed by the State of California and the United States government.

Potency of active ingredients are verified by laboratory testing, also disintegration testing is conducted at this time to insure compliance with U.S.P . standards.

The total product lot is then put in quarantine until the laboratory tests are completed and the paperwork prepared for storage.

Each lot of the finished product is sampled at the manufacturing and packaging levels and these samples are retained for a minimum of the expected shelf life of the product plus one year. All documentation includes the appropriate lot number for subsequent tracking if necessary.

Each product meets all laboratory tests, verifying standards of identity, potency, quality, disintegration and purity.

The following methods of analysis are used: Association of Official Analytical Chemist ( AOAC) plus one of our proprietary methods which utilize high pressure liquidchromatography as final analysis.

Formulations can be tailor made for your business or your country, they can be an entirely new product or a modified one (some countries have higher or lower RDA recommended ) our manufacturing company can assist you in taking the necessary steps to achieve your custom made formulation and finalise the product, you just fill the form at the bottom of the page. Go to Questionaire

18.10.2007. 19:08