dry eczema drops 2006

Generic: dry eczema drops

Labeler: professional complementary health formulas
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name dry eczema drops 2006
Generic Name dry eczema drops
Labeler professional complementary health formulas
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

calcium sulfide 8 [hp_X]/59mL, clematis recta flowering top 4 [hp_X]/59mL, graphite 12 [hp_X]/59mL, oyster shell calcium carbonate, crude 30 [hp_X]/59mL, potassium sulfate 6 [hp_X]/59mL

Manufacturer
Professional Complementary Health Formulas

Identifiers & Regulatory

Product NDC 63083-2006
Product ID 63083-2006_ad4d42f3-6735-435c-8be0-e284f9a9d0a0
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2027-12-31
Marketing Start 1984-08-15

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 630832006
Hyphenated Format 63083-2006

Supplemental Identifiers

UNII
1MBW07J51Q 396421SP9F 4QQN74LH4O 2E32821G6I 1K573LC5TV

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dry eczema drops 2006 (source: ndc)
Generic Name dry eczema drops (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 [hp_X]/59mL
  • 4 [hp_X]/59mL
  • 12 [hp_X]/59mL
  • 30 [hp_X]/59mL
  • 6 [hp_X]/59mL
source: ndc
Packaging
  • 59 mL in 1 BOTTLE, DROPPER (63083-2006-2)
source: ndc

Packages (1)

63083-2006-2 59 mL in 1 BOTTLE, DROPPER (63083-2006-2)

Ingredients (5)

calcium sulfide (8 [hp_X]/59mL) clematis recta flowering top (4 [hp_X]/59mL) graphite (12 [hp_X]/59mL) oyster shell calcium carbonate, crude (30 [hp_X]/59mL) potassium sulfate (6 [hp_X]/59mL)

Linked Drug Pages (1)

Dry Eczema Drops 2006 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ad4d42f3-6735-435c-8be0-e284f9a9d0a0", "openfda": {"unii": ["1MBW07J51Q", "396421SP9F", "4QQN74LH4O", "2E32821G6I", "1K573LC5TV"], "spl_set_id": ["72e775e7-e5fb-40fc-a96a-bc1b6015cc93"], "manufacturer_name": ["Professional Complementary Health Formulas"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59 mL in 1 BOTTLE, DROPPER (63083-2006-2)", "package_ndc": "63083-2006-2", "marketing_start_date": "19850815"}], "brand_name": "Dry Eczema Drops 2006", "product_id": "63083-2006_ad4d42f3-6735-435c-8be0-e284f9a9d0a0", "dosage_form": "LIQUID", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "63083-2006", "generic_name": "Dry Eczema Drops", "labeler_name": "Professional Complementary Health Formulas", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dry Eczema Drops", "brand_name_suffix": "2006", "active_ingredients": [{"name": "CALCIUM SULFIDE", "strength": "8 [hp_X]/59mL"}, {"name": "CLEMATIS RECTA FLOWERING TOP", "strength": "4 [hp_X]/59mL"}, {"name": "GRAPHITE", "strength": "12 [hp_X]/59mL"}, {"name": "OYSTER SHELL CALCIUM CARBONATE, CRUDE", "strength": "30 [hp_X]/59mL"}, {"name": "POTASSIUM SULFATE", "strength": "6 [hp_X]/59mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19840815", "listing_expiration_date": "20271231"}