Melissa
- Product NDC
- 48951-7222
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Melissa
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Substance
- ACONITUM NAPELLUS; ATROPA BELLADONNA; MELISSA OFFICINALIS; TOXICODENDRON PUBESCENS LEAF
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 48951-7222-1 | 10 g in 1 TUBE (48951-7222-1) | 2009-09-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Melissa | Uriel Pharmacy, Inc | 2025-09-16 | HUMAN OTC DRUG LABEL | 1 |