Rock Water
- Product NDC
- 57520-0366
- 11-digit product format
- 575200366
- Labeler code
- 57520
- Product ID
- 57520-0366_6e0bb85b-24a8-4723-b48b-f3d058f4cc33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Rock water
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Apotheca Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-05-03
- Marketing end
- 2022-09-06
- Substance
- WATER
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 57520-0366 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 57520-0366 | 57520-0366-1 | D | Discontinued by firm | | 2026-07-31 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57520-0366-1 | 57520036601 | 30 mL in 1 BOTTLE, DROPPER (57520-0366-1) | 30 ml | 2010-05-03 | 2022-09-06 | No | No | Current |