Label: HORMOSLIM- calcarea carbonica, nux vomica, sepia, spongia tosta, sulphur spray
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Contains inactivated NDC Code(s)
NDC Code(s): 68703-276-02 - Packager: Silver Star Brands
- 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 February 6, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- HPUS Active Ingredients:
- Uses*:
- Warnings:
- Directions:
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OTHER SAFETY INFORMATION
All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com. Contains no artificial flavors or colorants. No gluten added.
- Inactive Ingredients:
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HORMOSLIM
calcarea carbonica, nux vomica, sepia, spongia tosta, sulphur sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68703-276 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION 30 [hp_C] in 59 mL SEPIA OFFICINALIS WHOLE (UNII: 48GD5780QF) (SEPIA OFFICINALIS WHOLE - UNII:48GD5780QF) SEPIA OFFICINALIS WHOLE 30 [hp_C] in 59 mL SPONGIA OFFICINALIS WHOLE (UNII: 755U7L3M7Z) (SPONGIA OFFICINALIS WHOLE - UNII:755U7L3M7Z) SPONGIA OFFICINALIS WHOLE 30 [hp_C] in 59 mL STRYCHNOS NUX-VOMICA WHOLE (UNII: AB2NX17POS) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA WHOLE 30 [hp_C] in 59 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 30 [hp_C] in 59 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68703-276-02 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 02/06/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 02/06/2017 Labeler - Silver Star Brands (006070379) Registrant - Silver Star Brands (006070379) Establishment Name Address ID/FEI Business Operations King Bio 617901350 api manufacture(68703-276) , manufacture(68703-276)