510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K091419Substantially Equivalent

Vicks Powershot Dry Throat & Mouth Relief

Procter & Gamble Co., Mason OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K091419 is the FDA 510(k) clearance record for VICKS POWERSHOT DRY THROAT & MOUTH RELIEF, cleared for The Procter & Gamble Co. on under FDA product code LFD (Saliva, Artificial). FDA records list 33 510(k) clearances for The Procter & Gamble Co., from to . As of , FDA records show no recalls naming K091419.

Clearance record

Decision date
Received
(107 days to decision)
Product code
LFD Saliva, Artificial
Device class
Unclassified
Review panel
Unknown
Applicant
The Procter & Gamble Co. 8700 Mason-Montgomery Rd., Mason OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LFD

Trailing 12 months
1 clearance under product code LFD in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LFD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260