Artistry Hydra V Sheer Weightless Foundation Shade Ochre
- Product NDC
- 50390-221
- 11-digit product format
- 503900221
- Labeler code
- 50390
- Product ID
- 50390-221_cf82f578-3b04-defc-e053-2995a90ae373
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Amway Corp
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-09-23
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 40 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50390-221 | ARTISTRY HYDRA V SHEER WEIGHTLESS FOUNDATION SHADE OCHRE L2N1 (OCTINOXATE, ZINC OXIDE) CREAM [AMWAY CORP] | 2 | Legacy NDC | 20231022_bb9165e0-d802-45db-bb2a-5e512f3ab7bd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50390-221-00 | 50390022100 | 1 BOTTLE, PLASTIC in 1 CARTON (50390-221-00) > 30 mL in 1 BOTTLE, PLASTIC | 2017-09-23 | 0000-00-00 | No | No | Current |