EltaMD UV Daily Tinted SPF40
- Product NDC
- 72043-2269
- 11-digit product format
- 720432269
- Labeler code
- 72043
- Product ID
- 72043-2269_af5e1217-df99-4ea9-9e7a-5e80003ae285
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- zinc oxide and octinoxate sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- CP Skin Health Group, Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-10
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 75 g/1000g; g/1000g
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- 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.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72043-2269-1 | EltaMD UV Daily Tinted SPF40 | 48 g in 1 BOTTLE | LOTION | 48 | | 6 |
| 72043-2269-2 | EltaMD UV Daily Tinted SPF40 | 2 g in 1 PACKET | LOTION | 2 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72043-2269 | ELTAMD UV DAILY TINTED SPF40 (ZINC OXIDE AND OCTINOXATE SUNSCREEN) LOTION [CP SKIN HEALTH GROUP, INC.] | 5 | Legacy NDC, 2 package rows | 20231110_b9b5f3ef-bd38-4147-847a-af79da1d9cd6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72043-2269-1 | 72043226901 | 48 g in 1 BOTTLE (72043-2269-1) | 48 g | 2018-01-10 | 0000-00-00 | No | No | Current |
| 72043-2269-2 | 72043226902 | 2 g in 1 PACKET (72043-2269-2) | 2 g | 2022-07-06 | 0000-00-00 | No | No | Current |