Drugplain

Tobacco Leaf .1 g/mL

Tobacco Leaf · INJECTION · Allermed Laboratories, Inc.

No Recall History
Plain English

Tobacco Leaf is a injection containing tobacco leaf at .1 g/mL, taken cutaneous. Manufactured by Allermed Laboratories, Inc..

Key Facts

Brand Name
Tobacco Leaf
Generic Name
Tobacco Leaf
NDC Code (Product)
49643-022
Manufacturer
Allermed Laboratories, Inc.
Strength
.1 g/mL
Dosage Form
INJECTION
Route
CUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Marketing Status
Application #
BLA102211
Marketing Start
03/12/1974

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Indications For relief of occasional overexertion of the eyes. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Dosage & Administration

Dosage Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

Warnings

Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat. Tamper Evident Do not use this product if tamper evident strip is broken or removed from base of cap.

Frequently Asked Questions

What is Tobacco Leaf used for?

Tobacco Leaf contains Tobacco Leaf. It is a injection taken cutaneous. Consult your doctor for specific uses.

Is Tobacco Leaf a controlled substance?

Tobacco Leaf is not classified as a controlled substance by the DEA.

What is the generic name for Tobacco Leaf?

The generic name for Tobacco Leaf is Tobacco Leaf. There are 9 other brand versions of Tobacco Leaf.

What is the NDC code for Tobacco Leaf .1 g/mL?

The NDC (National Drug Code) for Tobacco Leaf .1 g/mL is 49643-022, listed by Allermed Laboratories, Inc..