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Lil' Drug Store Products, Inc.

FDA Regulatory Profile

Lil' Drug Store Products, Inc. has 0 FDA recalls, 4 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 3, 2024 · NAI
Latest 510(k)
Aug 17, 2010

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances3Oct 4, 2026Not statedCurrent
Inspections4Oct 27, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 3, 2024Cedar Rapids, IAFood/CosmeticsNo Action Indicated (NAI)3003491851
Jun 2, 2022Cedar Rapids, IADrugsVoluntary Action Indicated (VAI)3003491851
Aug 28, 2015Cedar Rapids, IADrugsNo Action Indicated (NAI)3003491851
Jun 9, 2010Cedar Rapids, IADrugsVoluntary Action Indicated (VAI)3003491851

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K101098REPLENS LONG-LASTING VAGINAL MOISTURIZER (35G TUBE WITH REUSABLE APPLICATOR) MODEL: 83035Aug 17, 2010
K101241REPLENS LONG-LASTING VAGINAL MOISTURIZER (PRE-FILLED APPLICATOR)Aug 17, 2010
K072414CRYOSTATApr 7, 2008

FDA data resources