LBEL
- Product NDC
- 14783-301
- 11-digit product format
- 147830301
- Labeler code
- 14783
- Product ID
- 14783-301_723f46da-0a2c-4f0b-94cb-503c5ef931bb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Oxybenzone, and Titanium dioxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Ventura International Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-04-19
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE
- Active strength
- 0 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 |
|---|---|---|---|---|---|
| 14783-301-02 | 2025-03-04 | C162847 | 48780-1 | 960f7f55-c788-8e05-e053-dbdaa90a074a | 15be4e55-1e26-49bc-9b7c-389746c3815a |
| 14783-301-04 | 2025-03-04 | C162847 | 48780-1 | 960f7f55-c788-8e05-e053-dbdaa90a074a | 15be4e55-1e26-49bc-9b7c-389746c3815a |
| 14783-301-06 | 2025-03-04 | C162847 | 48780-1 | 960f7f55-c788-8e05-e053-dbdaa90a074a | 15be4e55-1e26-49bc-9b7c-389746c3815a |
| 14783-301-02 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-c788-8e05-e053-dbdaa90a074a | 15be4e55-1e26-49bc-9b7c-389746c3815a |
| 14783-301-04 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-c788-8e05-e053-dbdaa90a074a | 15be4e55-1e26-49bc-9b7c-389746c3815a |
| 14783-301-06 | 2019-10-29 | C162847 | 48780-1 | 960f7f55-c788-8e05-e053-dbdaa90a074a | 15be4e55-1e26-49bc-9b7c-389746c3815a |