Label: ARALIA RACEMOSA MT- aralia racemosa liquid
- NDC Code(s): 66096-751-08
- Packager: OHM PHARMA INC.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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 Label Information
Updated December 28, 2021
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Caution: for manufacturing,processing or repacking only.
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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PRINCIPAL DISPLAY PANEL
NDC: 66096-751-08
ohm
PHARMA
Aralia Racemosa MT
0.250 Liters
Caution: for manufacturing,
processing or repacking only.
Active Ingredient: Ariala Racemosa MT
Inactive Ingredient: Ethanol 66%, Purified Water
Batch no. 40021
Retest Date: 11/2022
Distributed by: OHM Pharma
Mineral Wells, TX 76067
www.ohmpharma.com
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INGREDIENTS AND APPEARANCE
ARALIA RACEMOSA MT
aralia racemosa liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66096-751 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (ARALIA RACEMOSA ROOT - UNII:T90W4582DU) ARALIA RACEMOSA ROOT 0.25 in 0.25 L Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66096-751-08 0.25 L in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/01/2019 Labeler - OHM PHARMA INC. (030572478) Registrant - OHM PHARMA INC. (030572478) Establishment Name Address ID/FEI Business Operations OHM PHARMA INC. 030572478 manufacture(66096-751)