Good Morning IFSQN, we manufacturer breading's, dry batters and dry seasoning blends in bulk form. We sell to other businesses that use it as an ingredient for further processing. We sell 50lb brown bags and cases containing multiple 5lb plastic sacks.
1) Are we required to follow FDA Labeling Guidance and Rules if we are only selling B2B? (are we required to follow the PDP positioning, Net Weight - stating US and Metric -placed at 30% of bottom of PDP, Statement of Identity Rules, Font Size, Prominence, "Manufactured By", etc.). More specifically, Title 21, Chapter 1, Subchapter B, Part 101, Subpart A:
§ 101.1 Principal display panel of package form food. § 101.2 Information panel of package form food. § 101.3 Identity labeling of food in packaged form. § 101.4 Food; designation of ingredients. § 101.5 Food; name and place of business of manufacturer, packer, or distributor. § 101.7 Declaration of net quantity of contents. § 101.8 Vending machines.
2) The only exemption I could find is within subsection 101.9 (9) (j) which I believe is only in regard to the Nutritional Info, not all the other PDP FDA requirements. Meaning we are exempt from a Nutrition Facts panel. Can anyone confirm this?
§ 101.9 Nutrition labeling of food.
Subsection 101.9 (9) (j) states "Food products shipped in bulk form that are not for distribution to consumers in such form and that are for use solely in the manufacture of other foods or that are to be processed, labeled, or repacked at a site other than where originally processed or packed."
3) If we are selling B2B, who can possibly penalize our product labeling other than the business buying our product?
4) Would it make most sense that an agreement between both businesses would satisfy any labeling "requirements", does the FDA have any other B2B requirements listed somewhere?
Thank you for your help and answers!