e-z-gas ii

Generic: antacid/antiflatulent

Labeler: e-z-em, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name e-z-gas ii
Generic Name antacid/antiflatulent
Labeler e-z-em, inc.
Dosage Form GRANULE, EFFERVESCENT
Routes
ORAL
Active Ingredients

anhydrous citric acid 380 mg/g, dimethicone 10 mg/g, silicon dioxide 10 mg/g, sodium bicarbonate 550 mg/g

Manufacturer
E-Z-EM, INC.

Identifiers & Regulatory

Product NDC 10361-793
Product ID 10361-793_cee80987-94f6-6f1e-d2eb-45a137ec874d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 1986-05-01

Pharmacologic Class

Established (EPC)
calculi dissolution agent [epc] anti-coagulant [epc]
Mechanism of Action
acidifying activity [moa] calcium chelating activity [moa]
Physiologic Effect
decreased coagulation factor activity [pe] skin barrier activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10361793
Hyphenated Format 10361-793

Supplemental Identifiers

UNII
XF417D3PSL 92RU3N3Y1O ETJ7Z6XBU4 8MDF5V39QO
NUI
N0000175833 N0000175835 N0000175980 N0000008556 N0000175089 N0000010282

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 e-z-gas ii (source: ndc)
Generic Name antacid/antiflatulent (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 380 mg/g
  • 10 mg/g
  • 550 mg/g
source: ndc
Packaging
  • 50 POUCH in 1 BOX (10361-793-01) / 4 g in 1 POUCH
source: ndc

Packages (1)

10361-793-01 50 POUCH in 1 BOX (10361-793-01) / 4 g in 1 POUCH

Ingredients (4)

anhydrous citric acid (380 mg/g) dimethicone (10 mg/g) silicon dioxide (10 mg/g) sodium bicarbonate (550 mg/g)

Linked Drug Pages (1)

E-Z-GAS II ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cee80987-94f6-6f1e-d2eb-45a137ec874d", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089", "N0000010282"], "unii": ["XF417D3PSL", "92RU3N3Y1O", "ETJ7Z6XBU4", "8MDF5V39QO"], "spl_set_id": ["4e12e1cb-b033-076d-e054-00144ff8d46c"], "pharm_class_pe": ["Decreased Coagulation Factor Activity [PE]", "Skin Barrier Activity [PE]"], "pharm_class_epc": ["Calculi Dissolution Agent [EPC]", "Anti-coagulant [EPC]"], "pharm_class_moa": ["Acidifying Activity [MoA]", "Calcium Chelating Activity [MoA]"], "manufacturer_name": ["E-Z-EM, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (10361-793-01)  / 4 g in 1 POUCH", "package_ndc": "10361-793-01", "marketing_start_date": "19860501"}], "brand_name": "E-Z-GAS II", "product_id": "10361-793_cee80987-94f6-6f1e-d2eb-45a137ec874d", "dosage_form": "GRANULE, EFFERVESCENT", "pharm_class": ["Acidifying Activity [MoA]", "Alkalinizing Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Skin Barrier Activity [PE]"], "product_ndc": "10361-793", "generic_name": "Antacid/AntiFlatulent", "labeler_name": "E-Z-EM, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "E-Z-GAS", "brand_name_suffix": "II", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "380 mg/g"}, {"name": "DIMETHICONE", "strength": "10 mg/g"}, {"name": "SILICON DIOXIDE", "strength": "10 mg/g"}, {"name": "SODIUM BICARBONATE", "strength": "550 mg/g"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19860501", "listing_expiration_date": "20261231"}