PLAGENTRA MOTHERS BELLY
- Product NDC
- 68988-030
- 11-digit product format
- 689880030
- Labeler code
- 68988
- Product ID
- 68988-030_24737d57-e310-465f-ba48-784ee6082cbd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- OIL
- Route
- TOPICAL
- Labeler
- C.A Pharm Co., Ltd.
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-04-01
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN
- Active strength
- 1 mg/150mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 68988-030-01 | PLAGENTRA MOTHERS BELLY | 150 mL in 1 CARTON | OIL | 150 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68988-030 | PLAGENTRA MOTHERS BELLY (ALLANTOIN) OIL [C.A PHARM CO., LTD.] | 2 | Legacy NDC, 1 package rows | 20141205_8cd5c0f3-1f6d-489b-90d4-e0487a7f0b74.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68988-030-01 | 68988003001 | 150 mL in 1 CARTON | 150 ml | Historical |