fda
1 records
FDA Drug Recall: Smart Care HAND SANITIZER, Ethyl Alcohol 62%, packaged in 0.84 FL.OZ (25 mL), la
2020-10-21
Class I — Labeling: Not Elsewhere Classified. Container packaging is made, formed or filled to be misleading, resembling food and drink pouches
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fda_adverse
3 records
FDA AE Manufacturer: Ashtel Studios, Inc.
Drug adverse event reporter — Product: ISOPROPYL ALCOHOL
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FDA AE Manufacturer: Ashtel Studios Inc.
Drug adverse event reporter — Product: SODIUM FLUORIDE
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FDA AE Manufacturer: ASHTEL STUDIOS, INC
Drug adverse event reporter — Product: SODIUM FLUORIDE
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