sunscreen sprays
- Product NDC
- 82080-101
- 11-digit product format
- 820800101
- Labeler code
- 82080
- Product ID
- 82080-101_c61c3a8f-eaef-3110-e053-2995a90a05c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYLHEXYL METHOXYCINNAMATE
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Headblock LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-07-02
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE
- Active strength
- 5 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82080-101-01 | sunscreen sprays | 141 g in 1 BOTTLE | SPRAY | 141 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82080-101 | SUNSCREEN SPRAYS (ETHYLHEXYL METHOXYCINNAMATE) SPRAY [HEADBLOCK LLC] | 1 | Legacy NDC, 1 package rows | 20210703_c61c3a8f-eafd-3110-e053-2995a90a05c6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82080-101-01 | 82080010101 | 141 g in 1 BOTTLE (82080-101-01) | 141 g | 2021-07-02 | 0000-00-00 | No | No | Current |