Melissa
- Product NDC
- 48951-7222
- 11-digit product format
- 489517222
- Labeler code
- 48951
- Product ID
- 48951-7222_3eef31ef-39a4-3813-e063-6394a90a82af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Melissa
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- ACONITUM NAPELLUS; ATROPA BELLADONNA; MELISSA OFFICINALIS; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 30; 30; 1; 30 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Melissa
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS | 30 [hp_X]/g |
| ATROPA BELLADONNA | 30 [hp_X]/g |
| MELISSA OFFICINALIS | 1 [hp_X]/g |
| TOXICODENDRON PUBESCENS LEAF | 30 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U0NQ8555JD, WQZ3G9PF0H, YF70189L0N, 6IO182RP7A |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7222-1 | Melissa | 10 g in 1 TUBE | GEL | 10 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-7222-1 | 48951722201 | 10 g in 1 TUBE (48951-7222-1) | 10 g | 2009-09-01 | No | No | Current |