LBEL
- Product NDC
- 13537-404
- 11-digit product format
- 135370404
- Labeler code
- 13537
- Product ID
- 13537-404_7d3d469b-73f4-4516-9a5a-524698888c6f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Ensulizole, Octisalate, Octocrylene, and Oxybenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Ventura Corporation Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-12-13
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 0 g/mL; g/mL; g/mL; g/mL; g/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 13537-404-01 | 2025-04-25 | C162847 | 48780-1 | 97449f38-d085-f6ea-e053-dbdaa90aa703 | 08b4cb66-7a02-41cb-a592-c246146db020 |
| 13537-404-03 | 2025-04-25 | C162847 | 48780-1 | 97449f38-d085-f6ea-e053-dbdaa90aa703 | 08b4cb66-7a02-41cb-a592-c246146db020 |
| 13537-404-05 | 2025-04-25 | C162847 | 48780-1 | 97449f38-d085-f6ea-e053-dbdaa90aa703 | 08b4cb66-7a02-41cb-a592-c246146db020 |
| 13537-404-01 | 2019-11-13 | C162847 | 48780-1 | 97449f38-d085-f6ea-e053-dbdaa90aa703 | 08b4cb66-7a02-41cb-a592-c246146db020 |
| 13537-404-03 | 2019-11-13 | C162847 | 48780-1 | 97449f38-d085-f6ea-e053-dbdaa90aa703 | 08b4cb66-7a02-41cb-a592-c246146db020 |
| 13537-404-05 | 2019-11-13 | C162847 | 48780-1 | 97449f38-d085-f6ea-e053-dbdaa90aa703 | 08b4cb66-7a02-41cb-a592-c246146db020 |