Aftaseptic Analgesic Liquid

Manufacturer
Germa Products, LLC
Effective date
2026-10-09
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
daily-update
Hydrated at
2026-10-13 04:06:04

Label at a glance#

ProductAftaseptic Instant Pain Relief
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

For the temporary relief of pain associated with canker sores.

Dosage and administration

Use enclosed applicator brush Children 14 years of age to adult. Apply 2 brushstrokes 2 times a day to affected area of the mouth, gums or mucous membranes (throat). Do not rinse mouth after use. Children under 14 years of age consult a physician.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1% w/v

Purpose

OTC - PURPOSE SECTION

Analgesic

Uses

OTC - WHEN USING SECTION

For the temporary relief of pain associated with canker sores.

INDICATIONS & USAGE SECTION

for the temporary relief of pain associated with canker sores.

Warnings

WARNINGS SECTION

Alcohol warning: if you consume 3 or more alcoholic drinks everyday, consult with a specialist whether you should use Salicylic Acid or other pain reliever, fever reducers n Salicylic Acid may cause stomach bleeding.

Allergy alert: may cause a severe allergic reaction which may include: hives, facial swelling, asthma (wheezing), shock.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Flammable n Keep away from fire or flame. Do not use for teething or in children under 2 years of age
When using this product n avoid contact with eyes. Do not use longer than 1 week unless directed by a doctor. If pregnant or nursing contact a Doctor before using. Stop use and ask a doctor if condition persists or worsen
keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Other Information

OTHER SAFETY INFORMATION

Store between 15º to 30ºC (59º to 86ºF). Cap bottle tightly. Do not accept if safety seal is broken or missing. Cap bottle tightly. Keep this box for future doubts.

Directions

DOSAGE & ADMINISTRATION SECTION

Use enclosed applicator brush

Children 14 years of age to adult. Apply 2 brushstrokes 2 times a day to affected area of the mouth, gums or mucous membranes (throat). Do not rinse mouth after use. Children under 14 years of age consult a physician.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethyl Alcohol, propylene glycol, purified water, rhubarb.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Aftaseptic AftasepticAftaseptic

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130790933102055GTIN-13: 0790933102055
EAN-13: 0790933102055
GTIN-12: 790933102055
UPC-A: 790933102055
GTIN storage (14 digits): 00790933102055
Aftaseptic.jpg

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73635-710273635-7102-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
92025-10-10full-release2026-06-01 01:38:39
82024-10-15full-release2026-06-01 00:25:50

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
40d09de8-c64a-05c3-e063-6394a90afe11beb32fba-503a-f5e5-e053-2a95a90a57e52025-10-10WarningsExact identifier
spl set id: beb32fba-503a-f5e5-e053-2a95a90a57e5

Reported adverse events (FAERS/openFDA)#

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