Label: MUCUS-CLEAR JR. NIGHTTIME- chamomilla, cina, kali bic, kali carb, kali mur, pulsatilla liquid
- NDC Code(s): 68703-326-02
- 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 December 26, 2023
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- HPUS Active Ingredients
- Uses*
- Warnings
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Directions
Directions: Mix in 1/4 cup water and sip slowly, approximately 15 minutes before bed. Alternatively, drops may be taken directly into the mouth. Babies 6-11 months: 1 drop. Children 1-8: 1 drop per year of age. Children 9-14: Take 0.25 mL. Repeat every 4 hours during the night as needed until symptoms subside.
- OTHER SAFETY INFORMATION
- Inactive Ingredients
- KEEP OUT OF REACH OF CHILDREN
- PREGNANCY OR BREAST FEEDING
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MUCUS-CLEAR JR. NIGHTTIME
chamomilla, cina, kali bic, kali carb, kali mur, pulsatilla liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68703-326 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARTEMISIA CINA FLOWER (UNII: 28M1820ACT) (ARTEMISIA CINA FLOWER - UNII:28M1820ACT) ARTEMISIA CINA FLOWER 6 [hp_C] in 59 mL POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 30 [hp_C] in 59 mL POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 6 [hp_C] in 59 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 6 [hp_C] in 59 mL PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 6 [hp_C] in 59 mL MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA 6 [hp_C] in 59 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68703-326-02 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 05/13/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/13/2019 Labeler - Silver Star Brands (006070379) Registrant - Silver Star Brands (006070379) Establishment Name Address ID/FEI Business Operations OHM Pharma 030572478 manufacture(68703-326)
