bB Medicated Pain Relieving Oil

Manufacturer: BB BIOCHEM LABORATORIES, INC.
Effective date: 2014-11-01
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: full-release
Hydrated at: 2026-05-31 22:41:16

Label at a glance#

ProductbB Medicated Pain Relieving Oil

Active ingredientCAMPHOR (SYNTHETIC), LEVOMENTHOL, METHYL SALICYLATE, EUCALYPTUS OIL, CAPSAICIN, CAMPHOR (NATURAL)

Label structure17 sections

Indications and uses

Apply on Skin only ; for temporary relief of minor aches & pains of muscles & joints associated with sports and/or aging symptoms: ■ Simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Dosage and administration

If prone to allergic reaction from aspirin or salicylates, consult a doctor before use Adults and children12 years of age and over : ■ clean and dry affected area. ■ apply to affected area not more than 2 times a day. Children under 12 years of age : ■ consult a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Capsaicin natural extract 0.25 % as capsaicin

Camphor 3 %

Menthol 12 %

Methyl Salicylate 15 %

Eucalyptus Oil 15 %

Purpose

OTC - PURPOSE SECTION

Capsaicin natural extract ........................................... .Topical Analgesic

Camphor …………………………………………….........Topical Analgesic

Menthol ....................................................................... Topical Analgesic

Methyl Salicylate ..........................................................Topical Analgesic

Eucalyptus Oil ..............................................................Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Apply on Skin only; for temporary relief of minor aches & pains of muscles & joints associated with sports and/or aging symptoms:

■ Simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Warnings

WARNINGS SECTION

Keep out reach of children

If swallowed, get medical help or contact poison control center immediately.

Do not use

■ on wounds or damaged skin.

■ with a heating pad

■ with, or at the same time as, other external analgesic products.

■ if you are allergic to any ingredients of this product.

When using this product:

■ do not use otherwise than as directed.

■ avoid contact with eyes, mucous membranes or rashes.

Stop use and consult a doctor for:

■ rash, itching or excessive skin irritation develops.

■ conditions worsen.

■ symptoms persist for more than7 days.

■ symptoms clear up and occur again within a few days.

If swallowed, get medical help or contact poison control center immediately.

Directions and Allergy alert:

OTC - ASK DOCTOR SECTION

If prone to allergic reaction from aspirin or salicylates, consult a doctor before use

Adults and children12 years of age and over:

■ clean and dry affected area.

■ apply to affected area not more than 2 times a day.

Children under 12 years of age:

■ consult a doctor

Flammable and Safe Handling

SAFE HANDLING WARNING SECTION

keep away from fire or flame
do not use where ignition sparks happens
do not use in a confined space
do not incinerate or heat the bottle
do not expose bottle to temeprature exceeding 120 degree F (48 degree C)

Do NOT use:

OTC - DO NOT USE SECTION

on wounds or damaged skins.
with a heating pad.
if you are allergic to any ingredients of this product

When using this product:

OTC - WHEN USING SECTION

do not use otherwise than directed to.
avoid contact with the eyes, mucous membranes or rashes.
do not bandage tightly.
do not use on open wounds

Stop use and ask a doctor if any of the following happens:

OTC - STOP USE SECTION

rash, itching or excessive skin irritation develops
conditions worsen
symptoms persist for more than 7 days
symptoms clear up and return again within a few days

Pregancy or Breast Feeding.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breastfeeding, consult with your physician or a healthcare provider before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

If swallowed, get medical help or contact poison control center immediately.

Children under 12 years of age:

OTC - ASK DOCTOR SECTION

■ consult a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water, Ethanol, Cetyl alcohol, Polysorbate 80, Sorbitan monolaurate, Isopropyl myristate.

Other Information

OTHER SAFETY INFORMATION

■ Due to its unique formulation, the solution can turn into different levels of white translucent, milky cloudiness at warmer temperatures; This is totally normal. Upon returning to cooler temperatures it should regain its typical transparency state.

■ Avoid storing product in direct sunlight.

■ Protect product from excessive moisture.

Principle Display Panel-Extra Strength-Capsaicin 0.25/100

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC#61079-025-13

bB Medicated Oil Pain Reliever

Extra Strength

0.5 FL. OZ. (13 mL)

bB BioChem Laboratories, Inc.

Distributed by

bB BioChem Laboratories, Inc.

Santa Ana, CA 92705

bB BioChemUSA.com

Extra Strength Capsaicin 0.25/100

Carton-Extra Strenght- Capsaicin 0.25/100

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children12 years of age and over:

clean and dry affected area.
apply to affected area not more than 2 times a day.

Children under 12 years of age:

consult a doctor

Principle Display Panel-Sensitive Strength-Capsaicin 0.14/100

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC#61079-014-13

bB Medicated Oil Pain Reliever

Sensitive Strength-Capsaicin 0.14/100

0.5 FL. OZ. (13 mL)

bB BioChem Laboratories, Inc.

Distributed by

bB BioChemLaboratories, Inc.

Santa Ana, CA 92705

bBBioChemUSA.com

Sensitive Strenght-Capsaicin 0.14/100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1598277	camphor 3 % / capsaicin 0.25 % / eucalyptus oil 15 % / menthol 12 % / methyl salicylate 15 % Topical Oil	PSN	8
1598277	camphor 30 MG/ML / capsaicin 2.5 MG/ML / Eucalyptus oil 150 MG/ML / menthol 120 MG/ML / methyl salicylate 150 MG/ML Topical Oil	SCD	8
1598277	camphor 3 % / capsaicin 0.25 % / eucalyptus oil 15 % / menthol 12 % / methyl salicylate 15 % Topical Oil	SY	8

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
473d070d-1c38-488e-b991-c4d1bf45aab8	Product name	1	20210201
dea2eded-d1e7-46bb-9a3d-f8dc20de6277	Product name	1	20190408
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61079-014-13	2020-01-31	C162847	48780-1	9d75b9d0-3a57-f424-e053-dadaa90a57ce	bB MEDICATED PAIN RELIEVING OIL APPLY ON SKIN ONLY
61079-025-13	2020-01-31	C162847	48780-1	9d75b9d0-3a57-f424-e053-dadaa90a57ce	bB MEDICATED PAIN RELIEVING OIL APPLY ON SKIN ONLY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61079-014-13	bB Medicated Pain Relieving Oil	13 g in 1 BOTTLE, GLASS	OIL	13		8
61079-025-13	bB Medicated Pain Relieving Oil	13 g in 1 BOTTLE, GLASS	OIL	13		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61079-014	BB MEDICATED PAIN RELIEVING OIL OIL [BB BIOCHEM LABORATORIES, INC.]	8	Legacy NDC, 1 package rows	20150105_07b43c31-a4d2-5c29-e054-00144ff88e88.zip
61079-025	BB MEDICATED PAIN RELIEVING OIL OIL [BB BIOCHEM LABORATORIES, INC.]	8	Legacy NDC, 1 package rows	20150105_07b43c31-a4d2-5c29-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
CAMPHOR (NATURAL)	ACTIVE INGREDIENT	N20HL7Q941	8
CAMPHOR (SYNTHETIC)	ACTIVE INGREDIENT	5TJD82A1ET	8
CAPSAICIN	ACTIVE INGREDIENT	S07O44R1ZM	8
EUCALYPTUS OIL	ACTIVE INGREDIENT	2R04ONI662	8
LEVOMENTHOL	ACTIVE INGREDIENT	BZ1R15MTK7	8
METHYL SALICYLATE	ACTIVE INGREDIENT	LAV5U5022Y	8
CAMPHOR (NATURAL)	ACTIVE MOIETY	N20HL7Q941	8
CAMPHOR (SYNTHETIC)	ACTIVE MOIETY	5TJD82A1ET	8
CAPSAICIN	ACTIVE MOIETY	S07O44R1ZM	8
EUCALYPTUS OIL	ACTIVE MOIETY	2R04ONI662	8
LEVOMENTHOL	ACTIVE MOIETY	BZ1R15MTK7	8
SALICYLIC ACID	ACTIVE MOIETY	O414PZ4LPZ	8
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	8
CETYL ALCOHOL	INACTIVE INGREDIENT	936JST6JCN	8
ISOPROPYL MYRISTATE	INACTIVE INGREDIENT	0RE8K4LNJS	8
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	8
SORBITAN MONOLAURATE	INACTIVE INGREDIENT	6W9PS8B71J	8
WATER	INACTIVE INGREDIENT	059QF0KO0R	8

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

bB Medicated Pain Relieving Oil
CETYL ALCOHOL
POLYSORBATE 80
SORBITAN MONOLAURATE
ISOPROPYL MYRISTATE
ALCOHOL
WATER
CAMPHOR (SYNTHETIC)
LEVOMENTHOL
METHYL SALICYLATE
SALICYLIC ACID
EUCALYPTUS OIL
CAPSAICIN
CAMPHOR (NATURAL)

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
61079-025	61079-025-13
61079-014	61079-014-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CETYL ALCOHOL	936JST6JCN	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
SORBITAN MONOLAURATE	6W9PS8B71J	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	ACTIB
LEVOMENTHOL	BZ1R15MTK7	ACTIB
METHYL SALICYLATE	LAV5U5022Y	ACTIB
EUCALYPTUS OIL	2R04ONI662	ACTIB
CAPSAICIN	S07O44R1ZM	ACTIB
CETYL ALCOHOL	936JST6JCN	IACT
POLYSORBATE 80	6OZP39ZG8H	IACT
SORBITAN MONOLAURATE	6W9PS8B71J	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
EUCALYPTUS OIL	2R04ONI662	ACTIB
CAPSAICIN	S07O44R1ZM	ACTIB
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB
METHYL SALICYLATE	LAV5U5022Y	ACTIB
LEVOMENTHOL	BZ1R15MTK7	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 4 · 187 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SOLUTION / INTRAVENOUS		900 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAMUSCULAR		1000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	SUSPENSION / OPHTHALMIC	0.5 %w/v		Exact identifier — unii candidate 20 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SUPPOSITORY / RECTAL	72.15 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
SORBITAN MONOLAURATE	SORBITAN MONOLAURATE	6W9PS8B71J	AEROSOL, FOAM / TOPICAL		341 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	INJECTION, SUSPENSION / INTRAMUSCULAR		4 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	TABLET, FILM COATED / ORAL	NA		Exact identifier — unii candidate 20 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	CAPSULE, COATED / ORAL	0.04 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
SORBITAN MONOLAURATE	SORBITAN MONOLAURATE	6W9PS8B71J	SUSPENSION / ORAL	2.5 mg/5ml		Exact identifier — unii candidate 12 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	35.75 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	POWDER, FOR SOLUTION / TOPICAL	40 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ISOPROPYL MYRISTATE	ISOPROPYL MYRISTATE	0RE8K4LNJS	SYSTEM / TRANSDERMAL		113 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / SUBCUTANEOUS	6.1 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	INJECTION, POWDER, FOR SUSPENSION / INTRA-ARTICULAR		5 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SPRAY, METERED / NASAL	0.1 mg/1ml		Exact identifier — unii candidate 78 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	AEROSOL, FOAM / RECTAL		17 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	CAPSULE, DELAYED RELEASE / ORAL		59 mg	Exact identifier — unii candidate 20 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVASCULAR	100 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SUPPOSITORY / VAGINAL	28 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
SORBITAN MONOLAURATE	SORBITAN MONOLAURATE	6W9PS8B71J	CREAM / TOPICAL	0.5 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	DROPS / OPHTHALMIC	0.05 %w/w		Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	POWDER / ORAL	66 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SOLUTION / ORAL		907 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	INJECTION, SOLUTION / INTRAVENOUS		1170 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL		34 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
ISOPROPYL MYRISTATE	ISOPROPYL MYRISTATE	0RE8K4LNJS	AEROSOL / TOPICAL	9.3 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, FOAM / TOPICAL		4504 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	INJECTION, SUSPENSION / SOFT TISSUE		4 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TOPICAL		541 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SOLUTION / AURICULAR (OTIC)	0.2 %w/w		Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	CAPSULE / ORAL	418.37 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAVENOUS		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ISOPROPYL MYRISTATE	ISOPROPYL MYRISTATE	0RE8K4LNJS	OIL / TOPICAL		213 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	8 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
SORBITAN MONOLAURATE	SORBITAN MONOLAURATE	6W9PS8B71J	SPRAY, METERED / NASAL		1 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	CAPSULE, COATED PELLETS / ORAL	2 mg		Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	CONCENTRATE / INTRAVENOUS		4680 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	AEROSOL, FOAM / VAGINAL	3 %w/w		Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	ELIXIR / ORAL	2.5 mg/15ml		Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	CAPSULE, EXTENDED RELEASE / ORAL		10 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	MOUTHWASH / BUCCAL	200 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	EMULSION / TOPICAL		34050 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / RESPIRATORY (INHALATION)	5 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	EMULSION / TOPICAL	NA		Exact identifier — unii candidate 20 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SOLUTION, GEL FORMING, EXTENDED RELEASE / OPHTHALMIC	0.05 %w/w		Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SUSPENSION/ DROPS / OPHTHALMIC		1 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	INJECTION, SUSPENSION / SUBCUTANEOUS	0.3 %w/v		Exact identifier — unii candidate 78 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAMUSCULAR		1 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	TABLET / ORAL	NA		Exact identifier — unii candidate 20 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
CETYL ALCOHOL	CETYL ALCOHOL	936JST6JCN	SUSPENSION / TOPICAL	2.01 %w/w		Exact identifier — unii candidate 20 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	SUSPENSION / RESPIRATORY (INHALATION)		1 mg	Exact identifier — unii candidate 78 equally ranked IID candidates
POLYSORBATE 80	POLYSORBATE 80	6OZP39ZG8H	GEL / TOPICAL		12 mg	Exact identifier — unii candidate 78 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
0bc4e3b7-24a6-435a-e054-00144ff88e88			07b43c31-a4d2-5c29-e054-00144ff88e88	2014-11-01	Warnings	Exact identifier spl id: 0bc4e3b7-24a6-435a-e054-00144ff88e88 spl set id: 07b43c31-a4d2-5c29-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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