Wolf Daily Moisturizier SPF 15
- Product NDC
- 63148-008
- 11-digit product format
- 631480008
- Labeler code
- 63148
- Product ID
- 63148-008_c906efd9-39f7-4ce5-bbf2-2a280d095438
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Oxybenzone, Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Apollo Health and Beauty Care Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-06-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OXYBENZONE; ZINC OXIDE
- Active strength
- 20 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63148-008-04 | Wolf Daily Moisturizier SPF 15 | 118 mL in 1 TUBE | LOTION | 118 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63148-008 | WOLF DAILY MOISTURIZIER SPF 15 (OCTINOXATE, OXYBENZONE, ZINC OXIDE) LOTION [APOLLO HEALTH AND BEAUTY CARE INC.] | 1 | Legacy NDC, 1 package rows | 20180604_6f806d1d-c5f0-4a87-87f7-aa81033ae3b1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63148-008-04 | 63148000804 | 118 mL in 1 TUBE (63148-008-04) | 118 ml | 2018-06-01 | 0000-00-00 | No | No | Current |