Soothe

Manufacturer: Bausch & Lomb Incorporated
Effective date: 2024-09-20
Label type: HUMAN OTC DRUG LABEL
Version: 10
Source: full-release
Hydrated at: 2026-06-01 00:19:59

Label at a glance#

ProductSoothe

Active ingredientGLYCERIN, PROPYLENE GLYCOL

Label structure9 sections

Indications and uses

relieves dryness of the eye prevents further irritation

Dosage and administration

to open, completely twist off tab instill 1 to 2 drops in the affected eye(s) as needed discard dispenser immediately after use

Contacts and useful links#

PhoneLabel contact1-800-553-5340

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Glycerin (0.6%)

Propylene glycol (0.6%)

Purpose

OTC - PURPOSE SECTION

Lubricant

Uses

INDICATIONS & USAGE SECTION

relieves dryness of the eye
prevents further irritation

Warnings

WARNINGS SECTION

For external use only
Do not use

if solution changes color or becomes cloudy
if single-unit dispenser is not intact

When using this product

OTC - WHEN USING SECTION

do not touch tip of container to any surface to avoid contamination
once opened, discard
do not reuse

Stop use and ask a doctor if

OTC - STOP USE SECTION

you experience eye pain, changes in vision, continued redness or irritation of the eye
condition worsens or persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

to open, completely twist off tab
instill 1 to 2 drops in the affected eye(s) as needed
discard dispenser immediately after use

Other information

SPL UNCLASSIFIED SECTION

store at 15 – 25 °C (59 – 77 °F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

boric acid, hydroxyalkylphosphonate, purified water, sodium alginate, sodium borate

Questions?

OTC - QUESTIONS SECTION

[phone icon] Call: 1-800-553-5340

Marketed by:
Bausch & Lomb Americas Inc.
Bridgewater, NJ 08807 USA

Soothe is a trademark of|
Bausch & Lomb Incorporated
or its affiliates.

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bausch & Lomb
Soothe®

Lubricant Eye Drops

PRESERVATIVE FREE

Dry Eye Therapy

Moisturizes
Comforts
Lasts
Recommended
for LASIK dryness*
30 Single-Use Vials

Sterile 0.02 FL OZ EA (0.6 mL EA)

3839601

SootheEyeDrops.com

Order No. 622219

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1098601	SOOTHE LUBRICANT EYE DROPS (Ophthalmic)	glycerin 6 MG/ML / propylene glycol 6 MG/ML Ophthalmic Solution [Soothe Lubricant Eye Drops]	SBD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
832115	glycerin 0.6 % / propylene glycol 0.6 % Ophthalmic Solution	PSN	10
1098601	Soothe Lubricant 0.6 % / 0.6 % Ophthalmic Solution	PSN	10
1098601	glycerin 6 MG/ML / propylene glycol 6 MG/ML Ophthalmic Solution [Soothe Lubricant Eye Drops]	SBD	10
832115	glycerin 6 MG/ML / propylene glycol 6 MG/ML Ophthalmic Solution	SCD	10
832115	glycerin 0.6 % / propylene glycol 0.6 % Ophthalmic Solution	SY	10
1098601	Soothe Lubricant Eye Drops (glycerin 0.6 % / propylene glycol 0.6 % ) Ophthalmic Solution	SY	10

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
GLYCERIN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
24208-495-28	Soothe	28 in 1 CARTON	SOLUTION/ DROPS	28	10
24208-495-28	Soothe	0.6 mL in 1 VIAL, SINGLE-USE	SOLUTION/ DROPS	0.6	10
24208-495-30	Soothe	0.6 mL in 1 VIAL, SINGLE-USE	SOLUTION/ DROPS	0.6	10
24208-495-30	Soothe	30 in 1 CARTON	SOLUTION/ DROPS	30	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
24208-495	SOOTHE (GLYCERIN AND PROPYLENE GLYCOL) SOLUTION/ DROPS [BAUSCH & LOMB INCORPORATED]	10	Current NDC, Legacy NDC, 4 package rows	20240922_fef002ea-c4bd-4486-a42e-1bbd9d73d28d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
GLYCERIN	ACTIVE INGREDIENT	PDC6A3C0OX	4
PROPYLENE GLYCOL	ACTIVE INGREDIENT	6DC9Q167V3	4
GLYCERIN	ACTIVE MOIETY	PDC6A3C0OX	4
PROPYLENE GLYCOL	ACTIVE MOIETY	6DC9Q167V3	4
BORIC ACID	INACTIVE INGREDIENT	R57ZHV85D4	4
SODIUM ALGINATE	INACTIVE INGREDIENT	C269C4G2ZQ	4
SODIUM BORATE	INACTIVE INGREDIENT	91MBZ8H3QO	4
WATER	INACTIVE INGREDIENT	059QF0KO0R	4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

Soothe
glycerin and propylene glycol
BORIC ACID
WATER
SODIUM ALGINATE
SODIUM BORATE
GLYCERIN
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
24208-495	24208-495-28, 24208-495-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BORIC ACID	R57ZHV85D4	IACT
WATER	059QF0KO0R	IACT
SODIUM ALGINATE	C269C4G2ZQ	IACT
SODIUM BORATE	91MBZ8H3QO	IACT
GLYCERIN	PDC6A3C0OX	ACTIB
PROPYLENE GLYCOL	6DC9Q167V3	ACTIB

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 30 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	CAPSULE / ORAL		160 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TROCHE / ORAL		525 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET, EXTENDED RELEASE / ORAL		627 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
BORIC ACID	BORIC ACID	R57ZHV85D4	SOLUTION/ DROPS / OPHTHALMIC		48 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SYRUP / ORAL	3 mg/1ml		Exact identifier — unii candidate 24 equally ranked IID candidates
BORIC ACID	BORIC ACID	R57ZHV85D4	SOLUTION/ DROPS / OPHTHALMIC		48 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TROCHE / ORAL		525 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SUSPENSION / ORAL		49 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET, EXTENDED RELEASE / ORAL		627 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SUSPENSION / ORAL		49 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM BORATE	SODIUM BORATE	91MBZ8H3QO	SOLUTION/ DROPS / OPHTHALMIC	1.1 %w/v		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SUSPENSION / ORAL		49 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET / ORAL		480 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LOZENGE / ORAL		1274 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SYRUP / ORAL	3 mg/1ml		Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	CAPSULE / ORAL		160 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LOZENGE / ORAL		1274 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SYRUP / ORAL	3 mg/1ml		Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET / ORAL		480 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TROCHE / ORAL		525 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM BORATE	SODIUM BORATE	91MBZ8H3QO	SOLUTION/ DROPS / OPHTHALMIC	1.1 %w/v		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	CAPSULE / ORAL		160 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LIQUID / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LOZENGE / ORAL		1274 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM BORATE	SODIUM BORATE	91MBZ8H3QO	SOLUTION/ DROPS / OPHTHALMIC	1.1 %w/v		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LIQUID / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET / ORAL		480 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
BORIC ACID	BORIC ACID	R57ZHV85D4	SOLUTION/ DROPS / OPHTHALMIC		48 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LIQUID / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET, EXTENDED RELEASE / ORAL		627 mg	Exact identifier — unii candidate 24 equally ranked IID candidates

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Soothe	GLYCERIN AND PROPYLENE GLYCOL	Bausch & Lomb Incorporated	fef002ea-c4bd-4486-a42e-1bbd9d73d28d	2024-09-20	Warnings	Exact identifier ndc (package): 24208-495-28 ndc (package): 24208-495-30 ndc (product): 24208-495 ndc11 (package): 24208049530 ndc11 (package): 24208049528 spl id: 22996336-b8b3-8ee6-e063-6394a90a8537 spl set id: fef002ea-c4bd-4486-a42e-1bbd9d73d28d

Reported adverse events (FAERS/openFDA)#

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