# K091419: Vicks Powershot Dry Throat & Mouth Relief

- Pathway: 510(k) (Traditional)
- Applicant: The Procter & Gamble Co.
- Decided: Aug 28, 2009 after 107 days
- Product code: LFD (Saliva, Artificial)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K810157 (1981). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K810157: Moi-Stir, Kingswood Laboratories, Inc. (1981) Summary page 2.
- K840807: Throat Moi-Stir, Kingswood Laboratories, Inc. (1984) Summary page 2.
- K822971: Saliva Substitute, Roxane Laboratories, Inc. (1982) Summary page 2.

## Most influential descendants
- K110116: Xeros Dry Mouth Pump (2011), 1 descendant of its own
- K173808: Voutia™ (2018), 0 descendants of its own

## Indications for use
Vicks Powershot Dry Throat and Mouth Relief Spray - For immediate and effective relief of dry throat and dry mouth by coating, moistening and lubricating. Vicks Powershot Dry Throat and Mouth Relief Liquid - For immediate and effective relief of dry throat and dry mouth by coating, moistening and lubricating.

Source page: https://510kreport.com/device/K091419
Methodology: https://510kreport.com/methodology
