Glovers Dandruff Control Medicine, Regular
- Product NDC
- 12022-007
- 11-digit product format
- 120220007
- Labeler code
- 12022
- Product ID
- 12022-007_08340897-23b3-f23b-e063-6294a90a4eb9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur
- Dosage form
- SUSPENSION
- Route
- TOPICAL
- Labeler
- J. Strickland & Co.
- Application
- M032
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2001-09-24
- Substance
- SULFUR
- Active strength
- 25 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Glovers Dandruff Control Medicine, Regular
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 25 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
| Rxcui | 247683 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 12022-007-00 | Glovers Dandruff Control Medicine, Regular | 81 mL in 1 BOTTLE | SUSPENSION | 81 | | 5 |
| 12022-007-00 | Glovers Dandruff Control Medicine, Regular | 1 in 1 CARTON | SUSPENSION | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12022-007 | GLOVERS DANDRUFF CONTROL MEDICINE, REGULAR (SULFUR) SUSPENSION [J. STRICKLAND & CO.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20231021_18700036-11ec-4370-bcc6-b9e2c732e7d9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 12022-007-00 | 12022000700 | 1 BOTTLE in 1 CARTON (12022-007-00) / 81 mL in 1 BOTTLE | 1 bottle | 2001-09-24 | 0000-00-00 | No | No | Current |