ACNE RELIEF
- Product NDC
- 0220-9101
- 11-digit product format
- 002209101
- Labeler code
- 0220
- Product ID
- 0220-9101_06ea67d8-b617-776b-e063-6294a90a3185
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM BROMIDE, SYZYGIUM JAMBOS SEED, SELENIUM
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2022-05-16
- Substance
- POTASSIUM BROMIDE; SELENIUM; SYZYGIUM JAMBOS SEED
- Active strength
- 30; 6; 6 [hp_C]/1; [hp_C]/1; [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ACNE RELIEF
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM BROMIDE | 30 [hp_C]/1 |
| SELENIUM | 6 [hp_C]/1 |
| SYZYGIUM JAMBOS SEED | 6 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | OSD78555ZM, H6241UJ22B, 97P0H45869 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-9101-43 | ACNE RELIEF | 80 in 1 TUBE | PELLET | 80 | | 2 |
| 0220-9101-43 | ACNE RELIEF | 3 in 1 BOX | PELLET | 3 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-9101 | ACNE RELIEF (POTASSIUM BROMIDE, SYZYGIUM JAMBOS SEED, SELENIUM) PELLET [BOIRON] | 2 | Current NDC, Legacy NDC, 2 package rows | 20231005_df21b4e0-8c14-1c4d-e053-2995a90a74c7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-9101-43 | 00220910143 | 3 TUBE in 1 BOX (0220-9101-43) / 80 PELLET in 1 TUBE | 3 tube | 2022-05-16 | 0000-00-00 | No | No | Current |