DailyMed label
20Lighter Crave Control
DailyMed label · 20Lighter Health & Wellness, LLC · version 5
Key facts
| Product | 20Lighter Crave Control |
|---|---|
| Labeler | 20Lighter Health & Wellness, LLC |
| Document type | HUMAN PRESCRIPTION DRUG LABEL |
| Active ingredients | ACETYL COENZYME A, ADENOSINE TRIPHOSPHATE, ALCALIGENES FAECALIS, ALDOSTERONE, .ALPHA.-TOCOPHEROL, ANDROSTERONE, ANEMONE PATENS, ANTIMONY TRISULFIDE, ARTEMISIA CINA FLOWER, BERBERIS VULGARIS ROOT BARK, BLACK COHOSH, BRYONIA ALBA ROOT and 48 more |
| Active ingredient UNIIs | 00543AP1JV, 00IF91KFKQ, 05KB30NGW2, 076WHW89TW, 0B27814T7X, 0B4FDL9I6P, 0YPR65R21J, 1NM3M2487K, 1TH8Q20J0U, 269XH13919, 27YLU75U4W, 28M1820ACT and 50 more |
| Route | ORAL |
| NDC package codes | 70418-001-02, 70418-001-01 |
| Effective date | May 20, 2016 |
| Set ID | 2c272405-837d-007f-e054-00144ff88e88 |
At a glance
- 1–9 NDC package codes
- 10–99 Active ingredients
- 1–9 Manufacturing establishments listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About DailyMed drug labels
DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.
Source: U.S. National Library of Medicine (NLM), DailyMed · Source date: