Ultra V IDEBENONE SUNBLOCK
- Product NDC
- 71975-070
- 11-digit product format
- 719750070
- Labeler code
- 71975
- Product ID
- 71975-070_a6ead0b4-3f2a-49fd-8ef1-d12130e1dc26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, AVOBENZONE, ENSULIZOLE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Ultra V Co., Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-02
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; AVOBENZONE; ENSULIZOLE
- Active strength
- 5 g/50mL; g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71975-070-02 | 71975007002 | 1 TUBE in 1 CARTON (71975-070-02) > 50 mL in 1 TUBE (71975-070-01) | 1 tube | 2018-01-02 | 0000-00-00 | No | No | Current |