hims
- Product NDC
- 71730-042
- 11-digit product format
- 717300042
- Labeler code
- 71730
- Product ID
- 71730-042_619619ab-05ce-c750-e053-2a91aa0aa152
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Minoxidil 5%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Clubroom, Inc.
- Application
- ANDA075518
- Marketing category
- ANDA
- Marketing start
- 2017-11-01
- Marketing end
- 0000-00-00
- Substance
- MINOXIDIL
- Active strength
- 50 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 71730-042-08 | hims | 60 mL in 1 BOTTLE | LIQUID | 60 | | 4 |
| 71730-042-08 | hims | 1 in 1 BOX | LIQUID | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71730-042 | HIMS (MINOXIDIL 5%) LIQUID [CLUBROOM, INC.] | 4 | Legacy NDC, 2 package rows | 20171231_5d8460fc-cd6f-72af-e053-2a91aa0ad2f3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71730-042-08 | 71730004208 | 60 mL in 1 BOTTLE | 60 ml | Historical |