ActivOn Ultra Strength Arthritis
- Product NDC
- 51068-507
- 11-digit product format
- 510680507
- Labeler code
- 51068
- Product ID
- 51068-507_315fd1be-ae83-460e-96ac-e8117ded1dd7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol, Unspecified Form
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- Family First Pharmaceuticals, Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-02-15
- Marketing end
- 0000-00-00
- Substance
- MENTHOL, UNSPECIFIED FORM
- Active strength
- 0 g/g
- 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 |
|---|
| 51068-507-01 | ActivOn Ultra Strength Arthritis | 1 in 1 CARTON | STICK | 1 | | 1 |
| 51068-507-01 | ActivOn Ultra Strength Arthritis | 57 g in 1 CANISTER | STICK | 57 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51068-507 | ACTIVON ULTRA STRENGTH ARTHRITIS (MENTHOL, UNSPECIFIED FORM) STICK [FAMILY FIRST PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 2 package rows | 20170222_09d6b5a1-9223-4b60-b92d-7883a434a13e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 51068-507-01 | 51068050701 | 1 in 1 CARTON | Historical |