BonaDur
- Product NDC
- 70582-999
- 11-digit product format
- 705820999
- Labeler code
- 70582
- Product ID
- 70582-999_7b2018ec-84c3-6b95-e053-2a91aa0a2626
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- lidocaine
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- WebRx Pharmacy Palace
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-07-24
- Marketing end
- 0000-00-00
- Substance
- LIDOCAINE HYDROCHLORIDE
- Active strength
- 10 mg/mg
- 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 |
|---|
| 70582-999-74 | BonaDur | 10 mg in 1 BOTTLE, SPRAY | SPRAY | 10 | | 4 |
| 70582-999-74 | BonaDur | 1 in 1 BOX | SPRAY | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70582-999 | BONADUR (LIDOCAINE) SPRAY [WEBRX PHARMACY PALACE] | 4 | Legacy NDC, 2 package rows | 20181121_2e879abe-03fc-71aa-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70582-999-74 | 70582099974 | 10 mg in 1 BOTTLE, SPRAY | 10 mg | Historical |