TIESO RAPIDO PLUS
- Product NDC
- 73184-0083
- 11-digit product format
- 731840083
- Labeler code
- 73184
- Product ID
- 73184-0083_b927e5bd-3c87-444e-e053-2a95a90a34a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Ethylhexyl Salicylate, Titanium Dioxide, Benzalkonium Chloride
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- ANDIVA Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-12-01
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; BENZALKONIUM CHLORIDE; TITANIUM DIOXIDE; OCTISALATE
- Active strength
- 4 g/80mL; g/80mL; g/80mL; g/80mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73184-0083-1 | 73184008301 | 1 BOTTLE, SPRAY in 1 BOX (73184-0083-1) > 80 mL in 1 BOTTLE, SPRAY | 2020-12-01 | 0000-00-00 | No | No | Current |