lil drug store tylenol sinus severe

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride

Labeler: lil drug store products, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name lil drug store tylenol sinus severe
Generic Name acetaminophen, guaifenesin, and phenylephrine hydrochloride
Labeler lil drug store products, inc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Lil Drug Store Products, Inc

Identifiers & Regulatory

Product NDC 66715-9757
Product ID 66715-9757_459f7dbe-5021-08d1-e063-6294a90a8924
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2017-10-23

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 667159757
Hyphenated Format 66715-9757

Supplemental Identifiers

RxCUI
1243679
UNII
362O9ITL9D 04JA59TNSJ 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

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 lil drug store tylenol sinus severe (source: ndc)
Generic Name acetaminophen, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 200 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 POUCH in 1 CARTON (66715-9757-2) / 2 TABLET, COATED in 1 POUCH
  • 3 POUCH in 1 CARTON (66715-9757-3) / 2 TABLET, COATED in 1 POUCH
source: ndc

Packages (2)

66715-9757-2 2 POUCH in 1 CARTON (66715-9757-2) / 2 TABLET, COATED in 1 POUCH 66715-9757-3 3 POUCH in 1 CARTON (66715-9757-3) / 2 TABLET, COATED in 1 POUCH

Ingredients (3)

acetaminophen (325 mg/1) guaifenesin (200 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Tylenol Sinus Severe, Lil Drug Store, Tylenol Sinus Severe, CVP HEALTH, Tylenol Sinus Severe, TRAVEL BASIX, Lil Drug Store Tylenol Sinus Severe ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "459f7dbe-5021-08d1-e063-6294a90a8924", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "04JA59TNSJ", "495W7451VQ"], "rxcui": ["1243679"], "spl_set_id": ["88b68447-b016-4d5b-a5e3-c4ebccb14f8c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Lil Drug Store Products, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (66715-9757-2)  / 2 TABLET, COATED in 1 POUCH", "package_ndc": "66715-9757-2", "marketing_start_date": "20171023"}, {"sample": false, "description": "3 POUCH in 1 CARTON (66715-9757-3)  / 2 TABLET, COATED in 1 POUCH", "package_ndc": "66715-9757-3", "marketing_start_date": "20190815"}], "brand_name": "Lil Drug Store Tylenol Sinus Severe", "product_id": "66715-9757_459f7dbe-5021-08d1-e063-6294a90a8924", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "66715-9757", "generic_name": "Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "Lil Drug Store Products, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lil Drug Store Tylenol Sinus Severe", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171023", "listing_expiration_date": "20261231"}