Label: ICHTHAMMOL 20%- ichthammol ointment
- NDC Code(s): 63868-458-10
- Packager: Chain Drug Marketing Association, 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 May 23, 2023
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- DRUG FACTS
- Active ingredient
- Purpose
- KEEP OUT OF REACH OF CHILDREN
- Suggested Use
- Warnings
- Directions
- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- Other Information
- Packaging
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INGREDIENTS AND APPEARANCE
ICHTHAMMOL 20%
ichthammol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-458 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ICHTHAMMOL (UNII: NQ14646378) (ICHTHAMMOL - UNII:NQ14646378) ICHTHAMMOL 20 g in 100 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) LANOLIN (UNII: 7EV65EAW6H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-458-10 1 in 1 BOX 03/25/2019 1 28.3 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/19/2019 Labeler - Chain Drug Marketing Association, Inc. (011920774) Registrant - Trifecta Pharmaceuticals USA (079424163)