NDC | 60512-6009-0 |
Set ID | 000cf6bc-9e52-4261-9c73-4087c5ba1142 |
Category | HUMAN OTC DRUG LABEL |
Packager | HOMEOLAB USA INC. |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENTS HPUS
- REFERENCES
- PURPOSE
- USES
- WARNINGS
-
DIRECTIONS
Chew tablets and let dissolve in mouth.
Do not use more than directed.
Do not take with food.
Repeat 3 times daily and reduce intake with improvement or as directed by a health professional.
Age Dose Adults and children 12 years of age and older 2 tablets Children 2 to 11 years of age 1 tablet Children under 2 years of age Ask a doctor - OTHER INFORMATION
- INACTIVE INGREDIENTS
- CARTON
-
INGREDIENTS AND APPEARANCE
ECZEMA REAL RELIEF
fumaria officinalis, natrum muriaticum, agaricus muscarius, petroleum, sepia, kali arsenicosum, alumina tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60512-6009 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL) (FUMARIA OFFICINALIS FLOWERING TOP - UNII:VH659J61ZL) FUMARIA OFFICINALIS FLOWERING TOP 6 [hp_C] SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CATION 6 [hp_C] AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY - UNII:DIF093I037) AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY 6 [hp_C] KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 6 [hp_C] SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2) SEPIA OFFICINALIS JUICE 6 [hp_C] POTASSIUM ARSENITE ANHYDROUS (UNII: BM2U42PAKI) (ARSENITE ION - UNII:N5509X556J) ARSENITE ION 6 [hp_C] ALUMINUM OXIDE (UNII: LMI26O6933) (ALUMINUM OXIDE - UNII:LMI26O6933) ALUMINUM OXIDE 6 [hp_C] Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score no score Shape ROUND Size 8mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60512-6009-0 90 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/25/2012 Labeler - HOMEOLAB USA INC. (202032533) Establishment Name Address ID/FEI Business Operations HOMEOLAB USA INC. 202032533 manufacture(60512-6009)