Daily SPF30
- Product NDC
- 70707-400
- 11-digit product format
- 707070400
- Labeler code
- 70707
- Product ID
- 70707-400_d294b3fc-c64a-bd6d-e053-2995a90af6d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octisalate 4.75%, Oxybenzone 4.25%, Octocrylene 2.80%, Avobenzone 3.005
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Face Reality Skin Care, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-05-03
- Marketing end
- 0000-00-00
- Substance
- OXYBENZONE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
- Active strength
- 0 g/g; g/g; g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70707-400 | DAILY SPF30 (OCTISALATE 4.75%, OXYBENZONE 4.25%, OCTOCRYLENE 2.80%, AVOBENZONE 3.005) CREAM [FACE REALITY SKIN CARE, LLC] | 8 | Legacy NDC | 20241205_3f2b463c-26a7-701f-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70707-400-01 | 70707040001 | 62.5 g in 1 TUBE (70707-400-01) | 62.5 g | 2012-05-03 | 0000-00-00 | No | No | Current |