- Product NDC
- 61016-0005
- Requested package NDC
- 61016-0005-0
- 11-digit product format
- 610160005
- Labeler code
- 61016
- Product ID
- 61016-0005_951cb4b7-01e6-31ee-e053-2995a90a149f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OCTISALATE, AVOBENZONE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Columbia Cosmetics Manufacturing, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-07-29
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; AVOBENZONE
- Active strength
- 75 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table| Captured / source date | Snapshot | Source SHA-256 |
|---|
| 2024-03-11 06:39 UTC · source 2024-03-08 | 1332a3947898… | d4bfe170f9cd… |
| 2022-08-30 03:57 UTC · source 2022-08-29 | fb8cb913e6d1… | eb8c232b6be0… |
| 2022-04-09 23:13 UTC · source 2022-04-08 | 86f5da6cb304… | a595104c45d7… |
| 2022-04-04 05:40 UTC · source 2022-04-01 | bd6a592717d7… | 303034d00443… |