Answer:
1 goes with C. 2 goes with B. 3 goes with A
Explanation:
BRAINLIEST?
No because your body still does need those nutrients
The answer you are are looking for is Regular heartbeat
Answer:
Our bodies deliberately send more blood to an erectile tissue between the two nostrils to increase its size and direct the air flowing through one of the nostrils. After a few hours, the airflow switches to the other nostril.
Explanation:
I’ll bet most people don’t realize that when you breathe through your nose, you do so more from one nostril than the other and your body knows to switch to the other nostril every few hours. I had no idea. I’m only aware of any difference in my nostrils when I’m congested!
This nasal cycle is controlled by the autonomic nervous system which also controls things we don’t think about like heart rate and breathing
Why do we do this? Some scientists believe the alternating airflow allows each nostril to maintain optimal moisture levels so no one side gets dried out. It may also protect against respiratory infections or allergies.
Others believe it’s tied to our olfaction or sense of smell. It’s possible that the quicker and slower airflow in each nostril optimizes us to the vast range of smells. Some smells take longer to detect and transmit to the brain.
Answer:
It would not be advisable to promote a product before they approve it since you do not know if they will validate it and you will spend on marketing for pleasure
Whether or not a new drug requires approval The FDA's dependence on the new drug fits an over-the-counter (OTC) monograph. OTC monographs specified conditions under which the FDA has predetermined that a medication will be safe and effective. Once an OTC monograph is finalized, medication devices can market OTC medications that conform to the monograph without FDA approval. The FDA also uses the application at its discretion to allow certain medications to be marketed without approval if they conform to tentative final monographs.
If a new medication does not meet a monograph, it will require FDA approval. To obtain FDA approval, drug manufacturers must conduct laboratory tests, animal and human clinical analyzes, and submit their information to FDA. The FDA will review the information and may then approve the medication if the agency determines the benefits of the medication plus the risks to the intended use. Marketing a new drug that is not compliant with an OTC monograph and without an FDA test is considered as marketing a new unapproved medication, which is a prohibited act under the Food, Drug and Cosmetic Act (FD&C Act).