Natureplex
- Product NDC
- 67234-024
- 11-digit product format
- 672340024
- Labeler code
- 67234
- Product ID
- 67234-024_c69046f5-7564-4cb2-a366-c04cc67a9a13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WITCH HAZEL and PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Natureplex LLC
- Application
- part346
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-03-18
- Marketing end
- 0000-00-00
- Substance
- WITCH HAZEL; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 1 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67234-024-01 | Natureplex Hemorrhoidal | 1 in 1 BOX | GEL | 1 | | 3 |
| 67234-024-01 | Natureplex Hemorrhoidal | 25 g in 1 TUBE | GEL | 25 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67234-024 | NATUREPLEX HEMORRHOIDAL (WITCH HAZEL AND PHENYLEPHRINE HYDROCHLORIDE) GEL [NATUREPLEX LLC] | 3 | Legacy NDC, 2 package rows | 20250101_0614c8ed-db34-4f32-bffa-891c3183ed1b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67234-024-01 | 67234002401 | 1 TUBE in 1 BOX (67234-024-01) > 25 g in 1 TUBE | 1 tube | 2014-03-18 | 0000-00-00 | No | No | Current |