Octinoxate, Zinc Oxide
- Product NDC
- 0869-0909
- 11-digit product format
- 008690909
- Labeler code
- 0869
- Product ID
- 0869-0909_e13dc711-69cc-4349-80a9-80098e13ccd8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-03-17
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 61 mg/mL; mg/mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0869-0909-26 | 00869090926 | 1 BOTTLE, PLASTIC in 1 BOX (0869-0909-26) > 118 mL in 1 BOTTLE, PLASTIC | 2016-03-17 | 0000-00-00 | No | No | Current |
| 0869-0909-30 | 00869090930 | 1 BOTTLE, PLASTIC in 1 BOX (0869-0909-30) > 177 mL in 1 BOTTLE, PLASTIC | 2016-03-17 | 0000-00-00 | No | No | Current |