Double Use Compact SPF 15 gold deluxe edition Medium 5
- Product NDC
- 14783-277
- Requested package NDC
- 14783-277-01
- 11-digit product format
- 147830277
- Labeler code
- 14783
- Product ID
- 14783-277_b5f80d1f-f8cd-70b4-e053-2995a90a86ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Titanium dioxide, Zinc Oxide
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Ventura International LTD
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-11-12
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE; OCTINOXATE
- Active strength
- 5 g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 14783-277-01 | 14783027701 | 10 g in 1 BOTTLE (14783-277-01) | 10 g | 2020-11-12 | 0000-00-00 | No | No | Current |