Lead acetate’s use as a color additive in cosmetic products will no longer be authorized in the US beginning on 6 January 2022, and the agency will exercise enforcement discretion for a year afterward. A 2018 hearing request from hair dye marketer Combe Inc. was denied by the agency on 7 October.
Nearly three years after objections from Combe Inc. forced the US Food and Drug Administration to stay its final rule to prohibit lead acetate’s use in hair coloring applications, the agency has denied the Grecian Formula marketer a hearing after determining it “did not raise issues of material fact.”
With the hearing denial announced on 7 October, the stay is lifted and the FDA’s final rule issued in...
Green Pharmaceuticals’ SnoreStop Nasal Spray, previously marketed as “NasoSpray,” still is available even though agency officials on multiple occasions for a month recommended a recall after an April inspection found “gross microbial contamination” in one lot.
Global beauty giant is working to adapt its approach to the prestige market to meet escalating competition, increased points of sale, and more knowledgeable consumers with new shopping habits, CFO Tracey Travis said at the Barclays Global Consumer Staples Conference.
Court order dismisses claims against Perrigo and Joseph Papa, its former CEO, with prejudice. Settlement also bars any claim against plaintiffs and class members, “whether arising under state, federal, common or foreign law,” alleging liability for losses.
Proposal to have panelists rate the strength of efficacy and safety evidence on a numeric scale also draws support in written comments on ways to optimize the advisory committee process.
Week after publishing safety alert about OPMS Black Liquid Kratom “linked to serious adverse health effects, including death,” FDA announced market research “to understand and characterize emergent risk/safety and perceived benefits reportedly linked to kratom and psychedelics.” But it withdrew the study 10 days later.
Semi-annual regulatory agenda of non-binding target dates also sets December goal for an NPRM to recognize N-acetyl-L-cysteine as a lawful dietary ingredient. Like IND exemptions rule, item on NAC included for first time in FDA’s list.
