trilocaine
Generic: lidocaine hydrochloride
Labeler: trifluent pharma llcDrug Facts
Product Profile
Brand Name
trilocaine
Generic Name
lidocaine hydrochloride
Labeler
trifluent pharma llc
Dosage Form
CREAM
Routes
Active Ingredients
lidocaine hydrochloride 41.2 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
73352-610
Product ID
73352-610_a7689557-109a-41e8-9f64-3c5991513739
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2024-06-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73352610
Hyphenated Format
73352-610
Supplemental Identifiers
RxCUI
UPC
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
trilocaine (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 41.2 mg/g
Packaging
- HOW SUPPLIED Trilocaine™4.12% Cream: 1 oz. (28.3 g) tube - NDC 73352-610-01 STORAGE AND HANDLING KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN. Store at 20°-25°C (68°-77°F) [see USP Controlled Room Temperature]. Protect from freezing.
- PRINCIPAL DISPLAY PANEL - 28.3 g Tube Pouch Label NDC: 73352-610-01 Rx only TRIFLUENT PHARMA™ Trilocaine™ (4.12% Lidocaine HCl Cream) Topical Anesthetic Net Wt. 1 oz. (28.3 g) Active ingredient: Lidocaine HCl, USP 4.12% Inactive ingredients: Alkyl (C12-15) benzoate, butylparaben, Carica papaya (papaya) fruit extract, Carthamus tinctorius (safflower) seed oil, cetyl alcohol, dimethicone, disodium EDTA, emulsifying wax, ethylparaben, glycerin, glycerol stearate, hydroxypropyl cellulose, isobutylparaben, Lavandula angustifolia (lavender) oil, methylparaben, PEG 100 stearate, phenoxyethanol, propylene glycol, propylparaben, purified water, sodium lactate, xanthan gum. Indications: For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritation. KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN Usual Adult Dosage: Apply a thin film to the affected area two or three times daily or as directed by a physician. Additional Product Information Enclosed. Caution: For external use only. Not for ophthalmic use. Store at 20°-25°C (68°-77°F) [see USP Controlled Room Temperature]. Protect from freezing. Distributed By: Trifulent Pharma San Antonio, TX 78213 610-01 Rev. 03/2024 FPO Data Matrix PRINCIPAL DISPLAY PANEL - 28.3 g Tube Pouch Label
Packages (0)
No package records.
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
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