MOISTURIZER
- Product NDC
- 61354-012
- 11-digit product format
- 613540012
- Labeler code
- 61354
- Product ID
- 61354-012_bcd4fedc-b3fd-e250-e053-2995a90ab1c0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- OXYGEN DEVELOPMENT, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-03-05
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 22 mg/100mg
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61354-012-01 | MOISTURIZER | 7.5 mg in 1 BOTTLE | CREAM | 7.5 | | 1 |
| 61354-012-01 | MOISTURIZER | 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 |
|---|
| 61354-012 | MOISTURIZER (ZINC OXIDE) CREAM [OXYGEN DEVELOPMENT, LLC] | 1 | Legacy NDC, 2 package rows | 20210310_bcd4fedc-b3fc-e250-e053-2995a90ab1c0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61354-012-01 | 61354001201 | 1 BOTTLE in 1 CARTON (61354-012-01) > 7.5 mg in 1 BOTTLE | 1 bottle | 2021-03-05 | 0000-00-00 | No | No | Current |