Dermesse Sunscreen SPF30 Medium Tint
- Product NDC
- 68723-331
- 11-digit product format
- 687230331
- Labeler code
- 68723
- Product ID
- 68723-331_4b4fda56-047d-4a29-a538-3a5a91c071aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Axia Medical Solutions, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-05-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 75 mg/g; mg/g
- 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 |
|---|
| 68723-331-02 | Dermesse Sunscreen SPF30 Medium Tint | 57 g in 1 BOTTLE | LOTION | 57 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68723-331 | DERMESSE SUNSCREEN SPF30 MEDIUM TINT (OCTINOXATE, ZINC OXIDE) LOTION [AXIA MEDICAL SOLUTIONS, LLC] | 4 | Legacy NDC, 1 package rows | 20210713_d22f1a00-121a-4d25-b956-21540e8908aa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68723-331-02 | 68723033102 | 57 g in 1 BOTTLE (68723-331-02) | 57 g | 2015-05-01 | 0000-00-00 | No | No | Current |