Country: Сједињене Америчке Државе
Језик: Енглески
Извор: NLM (National Library of Medicine)
BENZOIC ACID (UNII: 8SKN0B0MIM) (BENZOIC ACID - UNII:8SKN0B0MIM)
OHM PHARMA INC.
ORAL
OTC DRUG
USE: To be used according to standard homeopathic indications.
unapproved homeopathic
BENZOICUM ACIDUM- BENZOICUM ACIDUM PELLET OHM PHARMA 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._ ---------- BENZOICUM ACIDUM DRUG FACTS: ACTIVE INGREDIENTS: BENZOICUM ACIDUM CONTENT: Approx. 100 Pellets USE: To be used according to standard homeopathic indications. WARNINGS: KEEP OUT OF REACH OF CHILDREN. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. S TOP USE AND ASK A HEALTH CARE PROFESSIONAL if symptoms persist for more than 3 days or worsen. KEEP OUT OF REACH OF CHILDREN. DIRECTIONS: Dissolve 3-5 pellets under the tongue 3 times a day or as directed by a professional. OTHER INFORMATION: Store at room temperature. DO NOT USE if pellet dispenser seal is broken. INACTIVE INGREDIENTS:ORGANIC SUCROSE, lactose free. Manufactured according to the Homeopathic Pharmacopoeia of the United States (HPUS). PRODUCT OF USA. Mfg. By: OHM PHARMA, INC. Mineral Wells, TX 76067 WWW.OHMPHARMA.COM FDA Est # 3003231743 BENZOICUM ACIDUM The OTC Potency range from Benzoicum Acidum 6X-30X, 3C-30C, 200C, 1M. Standard bottle sizes for dilution-form can range from 30mL to 60mL. To be used according to standard homeopathic indications. BENZOICUM ACIDUM benzoicum acidum pellet PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:66096-799 ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH BENZOIC ACID (UNII: 8SKN0B0MIM) (BENZOIC ACID - UNII:8SKN0B0MIM) BENZOIC ACID 6 [hp_C] in 6 [hp_C] INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH SUCROSE (UNII: C151H8M554) PRODUCT CHARACTERISTICS COLOR white SCORE SHAPE ROUND SIZE 4mm FLAVOR IMPRINT CODE CONTAINS PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:66096-799- 01 6 [hp_C] in 1 TUBE; Type 0: Not a Combination Product 11/01/2019 OHM PHARMA INC. MARKETING INFORMATION MARKETING CATEGORY APPLICATION NUM Прочитајте комплетан документ