lacrisert
Generic: hydroxypropyl cellulose
Labeler: bausch & lomb incorporatedDrug Facts
Product Profile
Brand Name
lacrisert
Generic Name
hydroxypropyl cellulose
Labeler
bausch & lomb incorporated
Dosage Form
INSERT
Routes
Active Ingredients
hydroxypropyl cellulose (1600000 wamw) 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
24208-800
Product ID
24208-800_1e1a2eb7-408a-9cae-e063-6394a90a544b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018771
Listing Expiration
2026-12-31
Marketing Start
1981-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24208800
Hyphenated Format
24208-800
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
lacrisert (source: ndc)
Generic Name
hydroxypropyl cellulose (source: ndc)
Application Number
NDA018771 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- HOW SUPPLIED LACRISERT, a sterile, translucent, rod-shaped, water-soluble, ophthalmic insert made of hydroxypropyl cellulose, 5 mg, is supplied as follows: NDC 24208-800-60 in packages containing 60 unit doses (each wrapped in an aluminum blister), two reusable applicators, and a plastic storage container to store the applicators after use. Storage Store below 30°C (86°F).
- PRINCIPAL DISPLAY PANEL - 5 mg Carton of 60 NDC 24208-800-60 Rx only LACRISERT ® (hydroxypropyl cellulose ophthalmic insert) 5 mg FOR OPHTHALMIC USE ONLY Carton also contains two sterile applicators and a storage container. CONTAINS NO PRESERVATIVE 60 STERILE OPHTHALMIC INSERTS BAUSCH + LOMB 9421104 carton
Packages (0)
No package records.
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "1e1a2eb7-408a-9cae-e063-6394a90a544b", "openfda": {"unii": ["RFW2ET671P"], "rxcui": ["476707", "754512"], "spl_set_id": ["cc7a6a52-0b77-4df7-8403-dd21c1334f6c"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "Lacrisert", "product_id": "24208-800_1e1a2eb7-408a-9cae-e063-6394a90a544b", "dosage_form": "INSERT", "pharm_class": ["Demulcent Activity [MoA]", "Demulcent [EPC]"], "product_ndc": "24208-800", "generic_name": "hydroxypropyl cellulose", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacrisert", "active_ingredients": [{"name": "HYDROXYPROPYL CELLULOSE (1600000 WAMW)", "strength": "5 mg/1"}], "application_number": "NDA018771", "marketing_category": "NDA", "marketing_start_date": "19810601", "listing_expiration_date": "20261231"}