Label: SPONGILLA LACUSTRIS MT- spongilla lacustris tincture
- NDC Code(s): 66096-749-08
- 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 29, 2021
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- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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PRINCIPAL DISPLAY PANEL
NDC 66096-749-08
ohm
PHARMA
Spongilla lacustris MT
0.250
Caution: for manufacturing,
processing or repacking only.
Batch no. 38798
Retest Date: 11/2021
Active Ingredient: Spongilla Lacustris
Inactive Ingredient: Ethanol 64%, Purified Water
Distributed by: OHM Pharma
Mineral Wells, TX 76067
www.ohmpharma.com
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INGREDIENTS AND APPEARANCE
SPONGILLA LACUSTRIS MT
spongilla lacustris tinctureProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:66096-749 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SPONGILLA LACUSTRIS (UNII: 6SZ0G98BHM) (SPONGILLA LACUSTRIS - UNII:6SZ0G98BHM) SPONGILLA LACUSTRIS 1 [hp_X] 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:66096-749-08 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(66096-749)