- Product NDC
- 61016-0001
- Requested package NDC
- 61016-0001-1
- 11-digit product format
- 610160001
- Labeler code
- 61016
- Product ID
- 61016-0001_cf47ba4e-df5a-76d7-e053-2a95a90aa2f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Columbia Cosmetics Manufacturing, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-02-23
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 3 mg/100mL; mg/100mL; mg/100mL; mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|
| 2024-03-11 06:39 UTC · source 2024-03-08 | excluded package | package | 61016-0001 | 61016-0001-1 | I | Inactivated by FDA | | excluded / ndc_excluded.zip | 1332a3947898… | d4bfe170f9cd… |