DANDRUFF
- Product NDC
- 61480-310
- 11-digit product format
- 614800310
- Labeler code
- 61480
- Product ID
- 61480-310_d44a68e4-354a-6192-e053-2a95a90a49a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Bromatum, Kali Muriaticum, Kali Sulphuricum, Natrum Muriaticum, Sulphur, Calcarea Carbonica, Niccolum Sulphuricum.
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PLYMOUTH HEALTHCARE PRODUCTS LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-05-24
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM BROMIDE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SODIUM CHLORIDE; SULFUR; OYSTER SHELL CALCIUM CARBONATE, CRUDE; NICKEL SULFATE HEXAHYDRATE
- Active strength
- 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61480-310-01 | 61480031001 | 144 TABLET in 1 BOTTLE, PLASTIC (61480-310-01) | 144 tablet | 2017-05-24 | 0000-00-00 | No | No | Current |