Preparation H
- Product NDC
- 0573-2889
- 11-digit product format
- 005732889
- Labeler code
- 0573
- Product ID
- 0573-2889_d528363f-94d3-4234-8064-6eb50b198997
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- witch hazel
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- part346
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-04-12
- Marketing end
- 0000-00-00
- Substance
- WITCH HAZEL
- Active strength
- 200 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0573-2889-01 | 00573288901 | 77 g in 1 CANISTER (0573-2889-01) | 77 g | 2021-04-12 | 0000-00-00 | No | No | Current |