Kinfield Sunglow Luminizing Sunscreen SPF 30
- Product NDC
- 81750-030
- 11-digit product format
- 817500030
- Labeler code
- 81750
- Product ID
- 81750-030_f1e9261e-20e6-c1bc-e053-2a95a90ac1a6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kinfield Sunglow Luminizing Sunscreen SPF 30
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Kinfield, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-04-05
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 20 g/100g
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81750-030 | KINFIELD SUNGLOW LUMINIZING SUNSCREEN SPF 30 LOTION [KINFIELD, INC.] | 5 | Legacy NDC | 20241222_346409ee-ae61-463c-aea3-048b82cd9927.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81750-030-60 | 81750003060 | 1 TUBE in 1 PACKAGE (81750-030-60) > 60 g in 1 TUBE | 1 tube | 2021-06-14 | 0000-00-00 | No | No | Current |