Moisture Oyster

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Moisture Oyster
Generic name: GLYCERIN
Manufacturer: Moisture Oyster Inc
Product type: HUMAN OTC DRUG
SPL set ID: 4e45317a-437f-4d88-e063-6294a90a98d0
SPL ID: 4e452d3e-ff82-4d8c-e063-6294a90aa4c1
Version: 1
Effective date: 2026-03-30
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:38:24

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Moisture Oyster	openfda.brand_name
generic name		GLYCERIN	openfda.generic_name
manufacturer name		Moisture Oyster Inc	openfda.manufacturer_name
ndc	package	87105-100-10	openfda.package_ndc
ndc	product	87105-100	openfda.product_ndc
ndc11	package	87105010010	derived:openfda.package_ndc
rxcui		310541	openfda.rxcui
spl id		4e452d3e-ff82-4d8c-e063-6294a90aa4c1	id
spl set id		4e45317a-437f-4d88-e063-6294a90a98d0	set_id
unii		PDC6A3C0OX	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Do not use if solution changes color or becomes cloudy. If tamper evident ring is broken or missing. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. Stop use and ask a doctor if: you experience eye pain changes in vision continued redness or irritation of the eye the condition worsens or persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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