Alkmene Anti Spot pad
- Product NDC
- 71084-001
- 11-digit product format
- 710840001
- Labeler code
- 71084
- Product ID
- 71084-001_46881f19-442b-1afd-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Green Tea
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Mann & Schroeder GmbH
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-01-16
- Marketing end
- 0000-00-00
- Substance
- TEA TREE OIL
- Active strength
- 48 g/100g
- 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 |
|---|
| 71084-001-01 | Alkmene Anti Spot pad | 15 g in 1 BOTTLE | LIQUID | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71084-001 | ALKMENE ANTI SPOT PAD (GREEN TEA) LIQUID [MANN & SCHROEDER GMBH] | 3 | Legacy NDC, 1 package rows | 20170120_463f11de-8bf1-329d-e054-00144ff88e88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71084-001-01 | 71084000101 | 15 g in 1 BOTTLE | 15 g | Historical |