Natureplex, established in 2001, offers their own control brand, but is also very strong in private label and contract packaging of enemas, feminine hygiene douches, over-the-counter medications, and personal care products. Product categories include both drug and cosmetics.
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Expert Collections containing Natureplex
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Companies that have been granted at least 1 510(k) by the FDA since 2014. Companies tagged as #FDA510(K)
Latest Natureplex News
Jan 31, 2018
Natureplex recalls Walgreens pain and itch relief over failure to meet safety closure requirement Published 31 January 2018 Walgreens pain and itch relief cream recalled by Natureplex due to failure to meet child resistant closure requirement. The packaging is not child resistant as required by the Poison Prevention Packaging Act. The pain and itch relief cream contains lidocaine, posing a risk of poisoning to young children. Consumers should immediately place the recalled pain and itch relief cream out of the reach of children and return it to Walgreens for a full refund. The recalled Well at Walgreens Pain and Itch Relief Cream tube and packaging are orange with a purple stripe with "Maximum Strength," "Pain and Itch Relief Cream 4% Lidocaine" and "NET WT 2 OZ (56.7 grams)" printed in white on the front. The Well at Walgreens logo is located on the front upper right corner. The packaging contains the UPC bar code 3 11917 18962 8 on the back. The U.S. Consumer Product Safety Commission is charged with protecting the public from unreasonable risks of injury or death associated with the use of thousands of types of consumer products under the agency's jurisdiction. Deaths, injuries, and property damage from consumer product incidents cost the nation more than $1 trillion annually. CPSC is committed to protecting consumers and families from products that pose a fire, electrical, chemical or mechanical hazard. CPSC's work to ensure the safety of consumer products - such as toys, cribs, power tools, cigarette lighters and household chemicals – contributed to a decline in the rate of deaths and injuries associated with consumer products over the past 40 years. Federal law bars any person from selling products subject to a publicly-announced voluntary recall by a manufacturer or a mandatory recall ordered by the Commission.
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