NDC11 65753010839

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
65753-0108-39	65753-0108
65753-108-39	65753-108

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CoreTex Professional Outdoor Skin Protection Wallet	CORETEX PROFESSIONAL OUTDOOR SKIN PROTECTION WALLET	CoreTex Products Inc	f57bc089-405b-cdcd-e053-2995a90a9d12	2025-10-09	Warnings	Exact identifier ndc (package): 65753-108-39 ndc11 (package): 65753010839
Sun X SPF 50 Broad Spectrum Sunscreen Lip Balm	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, PETROLATUM	CoreTex Products, INC	c0355990-b842-47cd-e053-2a95a90a7c82	2023-11-20	Warnings	Exact identifier ndc (product): 65753-108

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.