Parker Laboratories, Inc. recalls

Parker Laboratories, Inc. recalls Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

Parker Laboratories recalls Redux Electrolyte Creme (Product Ref. 66-04) due to low viscosity. This may cause product to spread too easily, but no specific safety risks are described in the recall notice.

Parker Laboratories, Inc. recalls Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%), packaged in a) 2 fl oz/60 mL Pump bottles (NDC

Parker Laboratories recalls Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) due to CGMP deviations. Products sold in 2 fl oz/60 mL and 18 fl oz/550 mL pump bottles with specific lot numbers are affected.

Parker Laboratories, Inc. recalls Helix CBD Clinical Cream (Menthol 7.4%), packaged in a)3 gm pouches (NDC30775-054-01), b)2 fl. oz. tubes (NDC

Parker Laboratories recalls Helix CBD Clinical Cream (Menthol 7.4%) due to CGMP deviations. Products packaged in 3 gm pouches (NDC 30775-054-01) and 2 fl. oz. tubes (NDC 30775-054-02) may be affected.

Parker Laboratories, Inc. recalls Helix CBD Therapy Cream (Menthol 7.4%), packaged in a) 3 g pouch (NDC 30775-053-01), b) 2 fl. oz. tubes (NDC

Parker Laboratories recalls Helix CBD Therapy Cream (Menthol 7.4%) due to CGMP deviations. Products with specific NDC codes and expiration dates are affected. Consumers should contact the company for details.

Parker Laboratories, Inc. recalls Helix Tri-Active Therapy Cream (Camphor 3.2%, Menthol 7.4%, Methyl salicylate 12.5%), packaged in a) 3 fl. oz. roll-on

Parker Laboratories, Inc. recalls Helix Pain Relieving Cream (Menthol 7.4%), packaged in a) 5 gm pouch (NDC 30775-051-01), b) 3 fl. oz. roll-on (NDC

Parker Laboratories recalls Helix Pain Relieving Cream (Menthol 7.4%) due to CGMP deviations. Products sold with specific NDC codes and expiration dates are affected. Consumers should check their product labels for the listed NDC numbers and expiration dates.