Natural Defense Foundation
- Product NDC
- 71413-218
- 11-digit product format
- 714130218
- Labeler code
- 71413
- Product ID
- 71413-218_e98965d5-d220-6eb9-e053-2995a90ac3f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Titanium Dioxide, Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Baja Fur, S.A. de C.V.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-01-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 7 mg/g; mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71413-218-02 | 71413021802 | 1 TUBE in 1 CARTON (71413-218-02) > 30 g in 1 TUBE (71413-218-01) | 1 tube | 2022-01-01 | 0000-00-00 | No | No | Current |