Label: PLANTAIN BEESWAX COUGH RELIEF ointment
- NDC Code(s): 48951-8038-5
- Packager: Uriel Pharmacy Inc.
- 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 April 30, 2018
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- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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WARNINGS
Warnings: FOR EXTERNAL USE ONLY.
Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing. - QUESTIONS
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INGREDIENTS AND APPEARANCE
PLANTAIN BEESWAX COUGH RELIEF
plantain beeswax cough relief ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-8038 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LARIX DECIDUA RESIN (UNII: AD8LJ73GQF) (LARIX DECIDUA RESIN - UNII:AD8LJ73GQF) LARIX DECIDUA RESIN 1 [hp_X] in 1 g SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE 3 [hp_X] in 1 g DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (DROSERA ROTUNDIFOLIA - UNII:QR44N9XPJQ) DROSERA ROTUNDIFOLIA 4 [hp_X] in 1 g PETASITES HYBRIDUS ROOT (UNII: 97S2809V5R) (PETASITES HYBRIDUS ROOT - UNII:97S2809V5R) PETASITES HYBRIDUS ROOT 4 [hp_X] in 1 g PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) (PLANTAGO MAJOR LEAF - UNII:7DC28K241X) PLANTAGO MAJOR LEAF 4 [hp_X] in 1 g Inactive Ingredients Ingredient Name Strength OLIVE OIL (UNII: 6UYK2W1W1E) YELLOW WAX (UNII: 2ZA36H0S2V) LANOLIN (UNII: 7EV65EAW6H) WATER (UNII: 059QF0KO0R) CAMPHOR (NATURAL) (UNII: N20HL7Q941) GLYCERIN (UNII: PDC6A3C0OX) EUCALYPTUS OIL (UNII: 2R04ONI662) LAVENDER OIL (UNII: ZBP1YXW0H8) THYME OIL (UNII: 2UK410MY6B) SODIUM ALGINATE (UNII: C269C4G2ZQ) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SAGE OIL (UNII: U27K0H1H2O) CITRUS PARADISI SEED (UNII: 12F08874Y7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48951-8038-5 60 g in 1 TUBE; Type 0: Not a Combination Product 09/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 09/01/2009 Labeler - Uriel Pharmacy Inc. (043471163) Establishment Name Address ID/FEI Business Operations Uriel Pharmacy Inc. 043471163 manufacture(48951-8038)