LBIO BLOCK
- Product NDC
- 73068-9201
- 11-digit product format
- 730689201
- Labeler code
- 73068
- Product ID
- 73068-9201_aa7c6469-03b6-74a3-e053-2995a90ab512
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sun block Cream
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- LCELLS SA DE CV
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-11-15
- Marketing end
- 0000-00-00
- Substance
- OXYBENZONE; OCTISALATE; ALLANTOIN; HYALURONIC ACID; OCTINOXATE; AVOBENZONE; OCTOCRYLENE
- Active strength
- 2 g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73068-9201-6 | 73068920106 | 50 mL in 1 BOTTLE, DISPENSING (73068-9201-6) | 50 ml | 2019-11-15 | 0000-00-00 | No | No | Current |