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FDA source record Class II Terminated

Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Bosto...

Recall Date: 2022-05-11 Recalling Firm: EarthLab Inc Record Ref: F-1348-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Bosto... and names EarthLab Inc as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: EarthLab Inc
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2022-05-11
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Product Description & Identification

Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Boston Round bottle, Black serrated polypropylene dropper assembly with rubber bulb (2oz only) or Black serrated phenolic lid with polypropylene cone insert(4oz and larger), Clear neck band, Wise Woman Herbals label. Each size has the following UPCs: 2 oz UPC 7 48840 14269 5 4 oz UPC 7 48840 14270 1 8 oz UPC 7 48840 14271 8 16 oz UPC 7 48840 14272 5 32 oz UPC 7 48840 14273 2

Reason for Recall / Hazard Identified

The microbial test result is found to be out of specification due to high yeast and mold counts.

How to Check Whether Your Product Matches

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Consumer Action Recorded in the Source

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Distribution & Affected States

nationwide

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1348-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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