DR FROG PP SUN BLOCK
- Product NDC
- 22201-1040
- 11-digit product format
- 222011040
- Labeler code
- 22201
- Product ID
- 22201-1040_243ca685-56a5-4fd5-8476-e597b17aa7ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Charmzone Co Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-03-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 4 g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 22201-1040-1 | DR FROG PP SUN BLOCK | 50 mL in 1 TUBE | CREAM | 50 | | 1 |
| 22201-1040-2 | DR FROG PP SUN BLOCK | 1 in 1 CARTON | CREAM | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 22201-1040 | DR FROG PP SUN BLOCK (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [CHARMZONE CO LTD] | 1 | Legacy NDC, 2 package rows | 20180413_71206697-924c-43a4-9d11-1d14520e5192.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 22201-1040-1 | 22201104001 | 50 mL in 1 TUBE | 50 ml | Historical |
| 22201-1040-2 | 22201104002 | 1 in 1 CARTON | | Historical |