Ultra Glow Fade
- Product NDC
- 58318-008
- 11-digit product format
- 583180008
- Labeler code
- 58318
- Product ID
- 58318-008_61f59bc5-2f47-764a-e053-2991aa0acb19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydroquinone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Keystone Laboratories
- Application
- part358A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-04
- Marketing end
- 0000-00-00
- Substance
- HYDROQUINONE; PADIMATE O
- Active strength
- 2 g/102g; g/102g
- 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 |
|---|
| 58318-008-01 | Ultra Glow Fade | 102 g in 1 JAR | CREAM | 102 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58318-008 | ULTRA GLOW FADE (HYDROQUINONE) CREAM [KEYSTONE LABORATORIES] | 1 | Legacy NDC, 1 package rows | 20180104_61f59bc5-2f46-764a-e053-2991aa0acb19.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 58318-008-01 | 58318000801 | 102 g in 1 JAR | 102 g | Historical |