Wonder Intensive BBCream 21 (Light)
- Product NDC
- 70931-0005
- 11-digit product format
- 709310005
- Labeler code
- 70931
- Product ID
- 70931-0005_5f1b0b79-6a67-47ae-e053-2991aa0a02ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium dioxide, Zinc Oxide, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Octocrylene, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Adenosine, Arbutin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- DRAN CO.,LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-02-23
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; OCTOCRYLENE; OCTINOXATE; OCTISALATE; ADENOSINE; ARBUTIN
- Active strength
- 3 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 70931-0005-1 | Wonder Intensive BBCream 21 (Light) | 40 g in 1 TUBE | CREAM | 40 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70931-0005 | WONDER INTENSIVE BBCREAM 21 (LIGHT) (TITANIUM DIOXIDE, ZINC OXIDE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, OCTOCRYLENE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, ADENOSINE, ARBUTIN) CREAM [DRAN CO.,LTD] | 3 | Legacy NDC, 1 package rows | 20171129_3bbc61e1-72c5-6681-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70931-0005-1 | 70931000501 | 40 g in 1 TUBE | 40 g | Historical |