Publix
- Product NDC
- 41415-047
- Requested package NDC
- 41415-047-75
- 11-digit product format
- 414150047
- Labeler code
- 41415
- Product ID
- 41415-047_397279ac-be74-ab1c-e063-6394a90ae7f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Publix Super Markets Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1995-08-23
- Substance
- HYDROCORTISONE
- Active strength
- 1 g/100g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 41415-047 | 41415-047-75 | I | Inactivated by FDA | excluded / ndc_excluded.zip | e2bbac7714bc… | 27bdfed8d636… | |
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 41415-047 | 41415-047-75 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 9bebd1f3094a… | 5416666fcb17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Publix
- Brand name suffix
- Hydro
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| HYDROCORTISONE | 1 g/100g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| WI4X0X7BPJ | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 106258 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 41415-047-75 | 2021-12-02 | C162847 | 48780-1 | 9d75b9d1-0bc4-f424-e053-dadaa90a57ce | Publix Hydrocream |
| 41415-047-75 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-0bc4-f424-e053-dadaa90a57ce | Publix Hydrocream |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41415-047-75 | PublixHydro | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 41415-047-75 | PublixHydro | 28.4 g in 1 TUBE | CREAM | 28.4 | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 106258 | hydrocortisone 1 % Topical Cream | PSN | 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | 5 |
| 106258 | hydrocortisone 10 MG/ML Topical Cream | SCD | 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | 5 |
| 106258 | hydrocortisone 1 % (as hydrocortisone acetate 1.2 % ) Topical Cream | SY | 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | 5 |
| 106258 | hydrocortisone 1 % Topical Cream | SY | 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | 5 |
| 106258 | hydrocortisone 1 GM per 100 GM Topical Cream | SY | 29296b0f-0eed-4bb9-8727-c25c2bcf9fd6 | 5 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41415-047-75 | 41415004775 | 1 TUBE in 1 CARTON (41415-047-75) / 28.4 g in 1 TUBE | 1 tube | 2009-01-23 | 0000-00-00 | No | No | Current |