The attempt of the California Office of Environmental Health Hazard Assessment (OEHHA) to change the short-form warning has finally come to fruition. Since January 8, 2021 when OEHHA first proposed a revamp of the short-form warning, we have been awaiting a final version to make it through the comment periods and the Administrative Procedures Act’s timeframe. That time has finally arrived!
On December 6, 2024, OEHHA announced that rulemaking had been approved and the effective date for the regulation would be January 1, 2025. The biggest change—required for products manufactured and labeled as of January 1, 2028—is that the short-form warning will explicitly identify a specific Proposition 65 chemical substance. A primary intent, aside from providing the consumer more information, is to reduce the propensity of many manufacturers to use the short-form warning as a prophylactic to protect against possible lawsuits (should they have failed to note the presence of such a substance in an accessible location of their product).
Whereas, today the format of the warning is:
⚠️ WARNING: Cancer - www.P65Warnings.ca.gov
The same warning will, as of January 1, 2028, be of the form:
⚠️ WARNING: Cancer risk from exposure to [name of chemical]. See www.P65Warnings.ca.gov.
⚠️ WARNING: Can expose you to [name of chemical], a carcinogen. See www.P65Warnings.ca.gov.
So much for “short.” Some of the restrictions on the use of the warning include:
So, start reviewing your use of the short-form warning and determine whether it makes sense to do the work necessary to determine whether a warning is necessary. Make sure you have appropriate control over your supply chain to ensure consistency and compliance over time. The days of prophylactic warning labels for Prop 65 are over.
The original EU Packaging Directive 94/62/EC first came into being over 30 years ago, well before the new millennium’s Y2K issues demanded specifying the full four-digit year. In early January, the long-expected recast finally made it out of committee and into the regulatory regimen of the EU. Technically, the Packaging and Packaging Waste Regulation (EU) 2025/40 (PPWR) came into force on Feb 11 but the current Directive 94/62/EC is not repealed until August 12, 2026 (per Article 70). So there's an 18-month transition period.
Note that regardless of where your company is in the supply chain and if your packaging ends up in the EU, this regulation applies to one extent or another. PPWR applies to all levels of packaging, from transport to retail product and covers both B2B and B2C packaging.
One positive aspect of this regulation, which applies directly across all EU Member States, is that it pre-empts all the unique packaging-specific requirements in the various Member States like France, Italy, Sweden, etc. We’ll see how that works out.
After a (quick) readthrough here are some other critical aspects:
This will require the attention of your packaging development engineering team and potentially your marketing team as well, for the next several years as the European Commission begins the process of developing delegated acts to define the details.
This is on top of the attention your environmental compliance and engineering teams (and potentially numerous others) will have to spend on developments for ESPR and the Battery Regulation. If you haven’t already done so and want to keep the EU as a market, consider reassessing your staffing and expertise needs to manage the coming changes—as well as all the others coming from the EU, including recasts or significant updates to WEEE, REACH including upcoming PFAS and flame retardant restrictions and RoHS.
Recently, a proposed update to China RoHS—as noted in a previous column—went through a public comment period that would, among other things, expand the range of reportable (or restricted) substances to include the same four phthalates as were added to EU RoHS a decade ago. Two months after the public comment period ended, a review was held and the “expert group conducted a strict review of the technical content of the standard and agreed to submit the standard for approval” (per Google’s English translation of the notice).
Whether any of the public comments influenced the content of the draft standard is unclear, the notice provides no information about whether the content of the draft standard was changed. My biggest concern is whether manufacturers of products in the “Catalog” will have to test for the presence of the soon-to-be ten (assuming that change is accepted) restricted substances. My bet is that they will. How unfortunate and meaningless.
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