Over the Counter Medications, Brand Names Beginning with ‘A’, Page 15

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Abella Color Shade SPF 35 Dark (Octinoxate and Zinc Oxide)

For external use only. Do not use on damaged or broken skin. When using this product: keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of…

Prime Enterprises Inc.17 January 2020

Abella Color Shade SPF 35 Ebony (Octinoxate and Zinc Oxide)

For external use only. Do not use on damaged or broken skin. When using this product: keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of…

Prime Enterprises Inc.17 January 2020

Abella Color Shade SPF 35 Light (Octinoxate and Zinc Oxide)

For external use only. Do not use on damaged or broken skin. When using this product: keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of…

Prime Enterprises Inc.17 January 2020

Abella ColorShade SPF 35 Medium (Octinoxate and Zinc Oxide)

For external use only. Do not use on damaged or broken skin. When using this product: keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of…

Prime Enterprises Inc.17 January 2020

Abercrombie and Fitch Co. Hand Sanitizer (Alcohol)

Uses: Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available. Directions: Place enough product on hands to cover all…

Bocchi Laboratories7 May 2020

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FDA Medwatch

Nostrum Laboratories, Inc. Expands Voluntary Nationwide Recall of Metformin HCl Extended Release Tablets, USP 750 mg, Due to N-Nitrosodimethylamine (NDMA) Content Above the Acceptable Daily Intake (ADI) Limit
Sun, 24 Jan 2021. Nostrum Laboratories, Inc. is voluntarily recalling one lot of Metformin HCl Extended Release Tablets, USP 750 mg (generic equivalent to Glucophage Tablets) to the consumer level. The Metformin HCl Extended Release Tablets, USP 750 mg (generic…
Boston Scientific Announces LOTUS Edge™ Aortic Valve System Voluntary Recall and Product Discontinuation
Sun, 10 Jan 2021. Boston Scientific Corporation (NYSE: BSX) has announced it has initiated a global, voluntary recall of all unused inventory of the LOTUS Edge™ Aortic Valve System due to complexities associated with the product delivery system. The voluntary…

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.