Country: United States
Language: English
Source: NLM (National Library of Medicine)
MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) (MELISSA OFFICINALIS LEAF - UNII:50D2ZE9219)
Phytodyne Inc.
ORAL
OTC DRUG
For temporary relief of states of nervousness
unapproved homeopathic
MELISSA OFFICINALIS (N)- MELISSA OFFICINALIS TINCTURE PHYTODYNE INC. _Disclaimer: This homeopathic product has not been evaluated by the Food and Drug_ _Administration for safety or efficacy. FDA is not aware of scientific evidence to support_ _homeopathy as effective._ ---------- MELISSA OFFICINALIS Ø (N) USE For temporary relief of states of nervousness DIRECTIONS Adults and children above 12 years: 2-5 drops 1-3 times daily in pure water before meals. Consult a physician for use in children under 12 years of age. INGREDIENTS Melissa officinalis Ø (N) ALCOHOL: 65 TAMPER-EVIDENT Do not use if tamper evident strip is broken from base of cap. WARNING Ask a doctor if you are pregnant or nursing. Keep away from children. In case of overdose, call a medical professional. PRINCIPAL DISPLAY PANEL - 20 ML BOTTLE LABEL CERES Homeopathic Medicine Melissa officinalis Ø (N) Use: For temporay relief of states of nervousness Directions : Adults and children above 12 years: 2-5 drops 1-3 times daily in pure water before meals. Consult a physician for use in children under 12 years of age. 0.67 fl.oz. (20ml) Lot#:1234567A ® EXP: 99.9999 MELISSA OFFICINALIS (N) melissa officinalis tincture PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:13838-1451 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219) (MELISSA OFFICINALIS LEAF - UNII:50D2Z E9219) MELISSA OFFICINALIS LEAF 1 [hp_X] in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH ALCOHOL (UNII: 3K9958V90M) PRODUCT CHARACTERISTICS COLOR BROWN SCORE SHAPE SIZE FLAVOR IMPRINT CODE CONTAINS PACKAGING MARKETING START MARKETING END Phytodyne Inc. # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:13838- 1451-1 20 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 10/01/2005 MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUMBER OR MONOGRAPH CITATION MARKETING START DATE MARKETING END DATE UNAPPROVED HOMEOPATHIC 10/01/2005 LABE Read the complete document