MyChelle Dermaceuticals Sun Shield SPF 50 Medium/Dark
- Product NDC
- 72805-200
- 11-digit product format
- 728050200
- Labeler code
- 72805
- Product ID
- 72805-200_95c39a3b-767e-4835-a449-68af25e566bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- French Transit, Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-04-01
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 20 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 72805-200-30 | MyChelle Dermaceuticals Sun Shield SPF 50 Medium/Dark Protect | 1 in 1 BOX | LIQUID | 1 | | 1 |
| 72805-200-30 | MyChelle Dermaceuticals Sun Shield SPF 50 Medium/Dark Protect | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72805-200 | MYCHELLE DERMACEUTICALS SUN SHIELD SPF 50 MEDIUM/DARK PROTECT (ZINC OXIDE) LIQUID [FRENCH TRANSIT, LTD.] | 1 | Legacy NDC, 2 package rows | 20210401_964af507-34fd-4967-aab0-3c0e54949fbe.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72805-200-30 | 72805020030 | 1 BOTTLE, DROPPER in 1 BOX (72805-200-30) > 30 mL in 1 BOTTLE, DROPPER | 2021-04-01 | 0000-00-00 | No | No | Current |