Fluaid

Manufacturer: PRINCE OF PEACE ENTERPRISES INC.
Effective date: 2014-04-01
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-05-31 22:39:06

Label at a glance#

ProductFluaid

Active ingredientMenthol

Label structure13 sections

Contacts and useful links#

PhoneLabel contact1-510-887-1899

Websitewww.popus.com

www.popus.com

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Menthol 135 mg.................Oral Pain Reliever

OTC - PURPOSE SECTION

Uses For the temporary relief of sore throat

OTC - WHEN USING SECTION

When using this product

Do not exceed recommended dosage

OTC - ASK DOCTOR/PHARMACIST SECTION

Stop use and ask a doctor if

sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting
sore mouth symptoms do not improve in 7 days
irritation, pain, or redness persists or worsens

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of reach of children.

OTC - DO NOT USE SECTION

Do not use otherwise than as directed

WARNINGS SECTION

In the case of accidental overdose, seek professional assistance or contact a poison control center immediately.

OTC - QUESTIONS SECTION

Questions? 1-510-887-1899 Monday to Friday, 8 am - 5 pm Pacific Standard Time

www.popus.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton label

INDICATIONS & USAGE SECTION

UsesFor the temporary relief of sore throat

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 12 years of age and older	Place 1 bags in 6 oz of boiling water and stir. Allow liquid to cool, Drink up to 4 times daily or as directed by a doctor
Children under 12 years of age	Ask A doctor

INACTIVE INGREDIENT SECTION

Corydalis bungeana, Phragmites Root, Kudzu Root, Siler Root, Schizonepeta Flower, Lactose, Fragrant Angelica Root, Platycodon Root, Bupleurum Root, Perilla Leaf, and Apricot Seed

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62003-002-30	2019-11-27	C162847	48780-1	9855e2a2-33bd-60a7-e053-dbdaa90a05bd	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62003-002-30	Fluaid	3 g in 1 PACKET	GRANULE, FOR SOLUTION	3		5
62003-002-30	Fluaid	10 in 1 BOX	GRANULE, FOR SOLUTION	10		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62003-002	FLUAID (MENTHOL) GRANULE, FOR SOLUTION [PRINCE OF PEACE ENTERPRISES INC.]	5	Legacy NDC, 2 package rows	20140426_b0c115b5-58f6-4b5f-be00-c0bd9ac7f138.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Menthol	ACTIVE INGREDIENT	L7T10EIP3A	5
Menthol	ACTIVE MOIETY	L7T10EIP3A	5
Angelica dahurica root	INACTIVE INGREDIENT	1V63N2S972	5
APRICOT	INACTIVE INGREDIENT	269CJD5GZ9	5
Bupleurum chinense root	INACTIVE INGREDIENT	BMA22623YK	5
CORYDALIS BUNGEANA FLOWERING/FRUITING TOP	INACTIVE INGREDIENT	93W3R296YH	5
Lactose	INACTIVE INGREDIENT	J2B2A4N98G	5
Perilla frutescens leaf	INACTIVE INGREDIENT	T4L5881Y68	5
PHRAGMITES AUSTRALIS ROOT	INACTIVE INGREDIENT	BBJ7AOM815	5
PLATYCODON GRANDIFLORUM LEAF	INACTIVE INGREDIENT	2L64H2X8DY	5
PUERARIA MONTANA VAR. CHINENSIS ROOT	INACTIVE INGREDIENT	FQN0D1U235	5
Saposhnikovia divaricata root	INACTIVE INGREDIENT	8H84LFK2QD	5
SCHIZONEPETA TENUFOLIA SPIKE	INACTIVE INGREDIENT	2FN3BA1MZE	5

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Fluaid
menthol
Angelica dahurica root
Lactose
Bupleurum chinense root
APRICOT
PUERARIA MONTANA VAR. CHINENSIS ROOT
Saposhnikovia divaricata root
SCHIZONEPETA TENUFOLIA SPIKE
PLATYCODON GRANDIFLORUM LEAF
Perilla frutescens leaf
CORYDALIS BUNGEANA FLOWERING/FRUITING TOP
PHRAGMITES AUSTRALIS ROOT

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62003-002	62003-002-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Menthol	L7T10EIP3A	ACTIB
Angelica dahurica root	1V63N2S972	IACT
Lactose	J2B2A4N98G	IACT
Bupleurum chinense root	BMA22623YK	IACT
APRICOT	269CJD5GZ9	IACT
PUERARIA MONTANA VAR. CHINENSIS ROOT	FQN0D1U235	IACT
Saposhnikovia divaricata root	8H84LFK2QD	IACT
SCHIZONEPETA TENUFOLIA SPIKE	2FN3BA1MZE	IACT
PLATYCODON GRANDIFLORUM LEAF	2L64H2X8DY	IACT
Perilla frutescens leaf	T4L5881Y68	IACT
CORYDALIS BUNGEANA FLOWERING/FRUITING TOP	93W3R296YH	IACT
PHRAGMITES AUSTRALIS ROOT	BBJ7AOM815	IACT

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 · 36 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Lactose	LACTOSE	J2B2A4N98G	TABLET, CHEWABLE / ORAL		1412 mg	Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	SOLUTION / ORAL	1682 mg/15ml		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR	133 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CAPSULE, COATED, EXTENDED RELEASE / ORAL	NA		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	GRANULE, FOR SUSPENSION / ORAL	512.5 mg/5ml		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, EXTENDED RELEASE / ORAL	400 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS	133 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CAPSULE, EXTENDED RELEASE / ORAL	120 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	POWDER / VAGINAL	430 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, SUGAR COATED / ORAL	NA		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET / SUBLINGUAL		352 mg	Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET / ORAL	2500 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CREAM / VAGINAL	3 %w/w		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	FILM, EXTENDED RELEASE / TRANSDERMAL	675 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, COATED / ORAL	332.05 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, FILM COATED / ORAL	590 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	OINTMENT / TOPICAL	NA		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CAPSULE, COATED PELLETS / ORAL	135.2 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CAPSULE / ORAL	530 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	SOLUTION / RECTAL	8 %w/v		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	POWDER / RESPIRATORY (INHALATION)	90 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET / RECTAL	20 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION / INTRAMUSCULAR	203.5 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARY	193.8 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CAPSULE / RESPIRATORY (INHALATION)	44.4 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION, SOLUTION / INTRAVENOUS	0.45 %w/v		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS	133 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, FILM COATED, EXTENDED RELEASE / ORAL		620 mg	Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, DELAYED RELEASE / ORAL		160 mg	Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	SUPPOSITORY / VAGINAL	NA		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CAPSULE, DELAYED RELEASE / ORAL	231.84 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	POWDER, FOR SOLUTION / ORAL	NA		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	CONCENTRATE / ORAL	NA		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	INJECTION / INTRAVENOUS	203.5 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET, EFFERVESCENT / ORAL	96.5 mg		Exact identifier — unii candidate 36 equally ranked IID candidates
Lactose	LACTOSE	J2B2A4N98G	TABLET / BUCCAL	296.7 mg		Exact identifier — unii candidate 36 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
7dc7752a-ef40-40c3-8571-c8b1d6162469			b0c115b5-58f6-4b5f-be00-c0bd9ac7f138	2014-04-01	Warnings	Exact identifier spl id: 7dc7752a-ef40-40c3-8571-c8b1d6162469 spl set id: b0c115b5-58f6-4b5f-be00-c0bd9ac7f138

Reported adverse events (FAERS/openFDA)#

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