Visage Pro Peach Fuzz
- Product NDC
- 35192-047
- 11-digit product format
- 351920047
- Labeler code
- 35192
- Product ID
- 35192-047_eee05894-f11a-0eef-e053-2995a90a3f40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen Visage Pro Peach Fuzz 5
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- CA-Botana International
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-07-22
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3 g/100g; g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35192-047 | VISAGE PRO PEACH FUZZ (SUNSCREEN VISAGE PRO PEACH FUZZ 5) EMULSION [CA-BOTANA INTERNATIONAL] | 4 | Legacy NDC | 20241208_e64e1469-47ee-f069-e053-2a95a90a8aa3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35192-047-02 | 35192004702 | 113.4 g in 1 PACKAGE (35192-047-02) | 113.4 g | 2022-07-22 | 0000-00-00 | No | No | Current |