82767-005-03

Manufacturer
TEAMTRADE INC.
Effective date
2026-10-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-27 02:03:40

Label at a glance#

ProductSEROMEN RAZOR BUMPS
Active ingredientALLANTOIN
Label structure14 sections

Dosage and administration

Apply on the affected area as needed.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%

OTC - PURPOSE SECTION

Skin Protectant

USE

INDICATIONS & USAGE SECTION

Temporarily protects and helps relieve chapped or cracked skin.

WARNINGS SECTION

For external use only.

Do not use on children under 12 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

do not get into eyes.

OTC - STOP USE SECTION

Condition worsens.

Symptoms last more than 7 days or clear up and occur again within a few days.

OTC - DO NOT USE SECTION

Deep or puncture wounds.
Animal bites.

Serious burns.

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

Apply on the affected area as needed.

OTHER SAFETY INFORMATION

See on the bottom of the container for lot number and expiration date.

Protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Glycerin, Salicylic Acid, Polysorbate 20, Silica, Xanthan Gum, Fragrance (Parfum), Salix Alba (Willow) Bark Extract, Sodium Hydroxide, Benzyl Alcohol, Benzoic Acid, Sorbic Acid, Hexyl Cinnamal, Benzyl Salicylate, Coumarin, Alpha-Isomethyl Ionone, Geraniol, Linalool, Eugenol.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

Call (1-877-737-6267)

SEROMEN RAZOR BUMPS SOLUTION BOX

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RAZOR BUMPS BOXRAZOR BUMPS BOX

SEROMEN RAZOR BUMPS SOLUTION ROLL ON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RAZOR BUMPS TUBERAZOR BUMPS TUBE

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82767-00582767-005-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-06-10full-release2026-06-01 00:13:28

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
1a8d9bbc-f1b2-ad94-e063-6394a90a22761a8d858c-7e2c-0018-e063-6294a90a790e2024-06-10WarningsExact identifier
spl set id: 1a8d858c-7e2c-0018-e063-6294a90a790e

Reported adverse events (FAERS/openFDA)#

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