Country: United States
Language: English
Source: NLM (National Library of Medicine)
ALLOXANUM
Washington Homeopathic Products
ORAL
OTC DRUG
To relieve the symptoms of toothache. Indications: ALLOXANUM Toothache If symptoms persist/worsen or if pregnant/nursing, consult your practitioner.
unapproved homeopathic
ALLOXANUM- ALLOXAN LIQUID WASHINGTON HOMEOPATHIC PRODUCTS _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._ ---------- DRUG FACTS ACTIVE INGREDIENTS ALLOXANUM USES To relieve the symptoms of toothache. KEEP OUT OF REACH OF CHILDREN Keep this and all medicines out of reach of children. INDICATIONS Indications: ALLOXANUM Toothache STOP USE AND ASK DOCTOR If symptoms persist/worsen or if pregnant/nursing, consult your practitioner. DIRECTIONS Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner. INACTIVE INGREDIENTS Sucrose/Lactose PRINCIPAL DISPLAY PANEL The OTC potency range of ALLOXANUM is 6x–30x, 3c–30c, 200c, 1m, 10m, 50m, and CM. Availability is subject to change. All WHP single remedies are made to order; thus, the labels are printed on the same label stock, as the orders are filled. ‘Bottle Size,’ ‘Potency,’ and ‘Alcohol Percentage’ vary on the label depending on customer choice. Standard bottle sizes for dilution-form remedies are 15ml, 30ml, 50ml, and 100ml. ALLOXANUM alloxan liquid PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:719 19 -0 30 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH ALLO XAN (UNII: 6 SW5YHA5NG) (ALLOXAN - UNII:6 SW5YHA5NG) ALLOXAN 30 [hp_C] in 1 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH ALCO HO L (UNII: 3K9 9 58 V9 0 M) Washington Homeopathic Products WATER (UNII: 0 59 QF0 KO0 R) PRODUCT CHARACTERISTICS COLOR white (white) S CORE S HAP E S IZ E FLAVOR IMPRINT CODE CONTAINS PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:719 19 -0 30 - 0 7 15 mL in 1 VIAL, GLASS; Type 0 : No t a Co mbinatio n Pro duct 0 8 /0 4/20 15 2 NDC:719 19 -0 30 - 0 8 30 mL in 1 VIAL, GLASS; Type 0 : No t a Co m Read the complete document