Facial Sunscreen with Zinc SPF 50
- Product NDC
- 11822-1214
- 11-digit product format
- 118221214
- Labeler code
- 11822
- Product ID
- 11822-1214_8fc8d766-40e6-4423-b786-3d124309ff2f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate 7.50% Octisalate 5.00% Oxybenzone 6.00% Zinc Oxide 7.00%
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Rite Aid
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-03-17
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE
- Active strength
- 8 g/100g; g/100g; g/100g; g/100g
- 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 |
|---|
| 11822-1214-1 | Facial Sunscreen with Zinc SPF 50Daylogic | 28.3 g in 1 JAR | CREAM | 28.3 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-1214 | FACIAL SUNSCREEN WITH ZINC SPF 50 DAYLOGIC (OCTINOXATE 7.50% OCTISALATE 5.00% OXYBENZONE 6.00% ZINC OXIDE 7.00%) CREAM [RITE AID] | 1 | Legacy NDC, 1 package rows | 20180512_8fb6968e-c70a-4f6d-8558-7882d48c511e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 11822-1214-1 | 11822121401 | 28.3 g in 1 JAR | 28.3 g | Historical |