Label: BLADDER RELIEF (causticum, natrum muriaticum, nux vomica, pulsatilla- vulgaris, sepia, staphysagria, thuja occidentalis tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 43689-0016-1, 43689-0016-2 - Packager: Magni Company
- Category: HUMAN OTC 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 January 11, 2022
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- ACTIVE INGREDIENTS:
- USES:
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WARNINGS:
• If pregnant or breastfeeding, ask a health professional before use
• Keep out of reach of children
• In case of overdose, get medical help or contact a Poison Control Center right away
• Stop use and ask a doctor if symptoms persist for more than 7 days or worsen, or if you have symptoms of a urinary tract infection
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OTHER INFORMATION:
• Store tightly closed in a cool, dry place (59° - 86°F)
• Tamper sealed: Sealed for your protection. Do not use if seal is broken or missing
• The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United
States
• These statements are supported by the traditional homeopathic principles
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- INDICATIONS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
BLADDER RELIEF
causticum, natrum muriaticum, nux vomica, pulsatilla (vulgaris), sepia, staphysagria, thuja occidentalis tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43689-0016 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU) CAUSTICUM 12 [hp_X] SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 12 [hp_X] STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 12 [hp_X] PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) PULSATILLA VULGARIS WHOLE 12 [hp_X] SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE 12 [hp_X] DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) DELPHINIUM STAPHISAGRIA SEED 12 [hp_X] THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) Product Characteristics Color white Score no score Shape ROUND (Round convex) Size 6mm Flavor Imprint Code ML Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43689-0016-2 1 in 1 PACKAGE 06/12/2015 1 NDC:43689-0016-1 125 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/12/2015 Labeler - Magni Company (113501902) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43689-0016) , api manufacture(43689-0016) , label(43689-0016) , pack(43689-0016)
