PROVENCE CALENDULA AQUA SUN
- Product NDC
- 51346-433
- 11-digit product format
- 513460433
- Labeler code
- 51346
- Product ID
- 51346-433_cc3b890e-823f-4eb6-a857-4b746886df9f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octinoxate
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- NATURE REPUBLIC CO., LTD.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-12-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE
- Active strength
- 1 g/15g; g/15g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51346-433-02 | 51346043302 | 1 BOTTLE, PLASTIC in 1 CARTON (51346-433-02) > 15 g in 1 BOTTLE, PLASTIC (51346-433-01) | 2016-12-01 | 0000-00-00 | No | No | Current |