BlueStop Max
- Product NDC
- 82714-002
- 11-digit product format
- 827140002
- Labeler code
- 82714
- Product ID
- 82714-002_4835e6a9-c202-02eb-e063-6294a90a7ead
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- External Analgesic
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Clavel Corporation
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-01-10
- Substance
- LIDOCAINE HYDROCHLORIDE; MENTHOL, (+)-
- Active strength
- 40; 10 mg/g; mg/g
- Pharmacologic classes
- Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BlueStop Max
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIDOCAINE HYDROCHLORIDE | 40 mg/g |
| MENTHOL, (+)- | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V13007Z41A, C6B1OE8P3W |
| Rxcui | 1595624 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82714-002-01 | BlueStop Max | 85 g in 1 TUBE | CREAM | 85 | | 3 |
| 82714-002-01 | BlueStop Max | 1 in 1 CARTON | CREAM | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82714-002 | BLUESTOP MAX (EXTERNAL ANALGESIC) CREAM [CLAVEL CORPORATION] | 2 | Current NDC, 2 package rows | 20240117_f2277e27-868b-57ef-e053-2a95a90abf28.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82714-002-01 | 82714000201 | 1 TUBE in 1 CARTON (82714-002-01) / 85 g in 1 TUBE | 1 tube | 2023-01-10 | No | No | Historical |