Lansinoh Anti-itch
- Manufacturer
- Lansinoh Laboratories Inc | Dhaliwal Pharmaceuticals Laboratories, LLC
- Effective date
- 2024-12-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 00:48:13
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
| Active Ingredients | Purpose |
| Menthol 0.5% | Topical Analgesic |
OTC - ASK DOCTOR SECTION
Stop Use and ask a doctor
- if condition worsens
- if symptoms persist for more than 7 days
- Or if symptoms clear up and occur again withina few days
OTC - DO NOT USE SECTION
Do NOT use in or near mouth, or on breasts or nipples when breast feeding.
Pregnant women are advised to consult their physician before using any OTC drug product.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN
if swallowed, get medical help or contact a Poison Control Center right awau (1-800-222-1222)
OTC - PURPOSE SECTION
For temporary relief of itching
OTC - STOP USE SECTION
Stop use and ask a doctor
- If condition worsens
- If symptoms persists for more than 7 days
- Or if symptoms clear up and occur again within a few days
WARNINGS SECTION
Warnings
For external use only
Avoid contact withthe eyes
DOSAGE & ADMINISTRATION SECTION
Directions
- For adults and children 2 years and older
- Apply externally to the affected area, no more than 3-4 times daily
INACTIVE INGREDIENT SECTION
Inactive Ingredients:
Aloe Barbadensis Leaf Juice, Avena Sativa (Oat) Meal Extract, Caprylyl Glycol, Carbomer, Cetearyl Olivate, Cucumis Sativus Fruit Extract, Cyclopentasiloxane, Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Glycerin, Hyaluronic Acid, Hydrolyzed Jojoba Esters, Hydroxyacetophenone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isopropyl Palmitate, Polysorbate 60, Prunus Armeniaca (Apricot) Kernel Oil), Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Benzoate, Potassium Sorbate, Sodium Chloride, Sodium Hydroxide, Sorbitan Isostearate, 1,2-Hexanediol, Sorbitan Olivate, Squalane, Water (Eau, Aqua).
INDICATIONS & USAGE SECTION
Uses
For temporary relief of itching
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53997-002-01 | Lansinoh Anti-itch | 125 mL in 1 TUBE | CREAM | 125 | 2 | |
| 53997-002-02 | Lansinoh Anti-itch | 1 in 1 CARTON | CREAM | 1 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Lansinoh Anti-itch
- Menthol 0.5%
- CUCUMBER
- POTASSIUM SORBATE
- SODIUM HYDROXIDE
- DIMETHICONE
- CYCLOMETHICONE 5
- GLYCERIN
- SQUALANE
- JOJOBA OIL
- ISOPROPYL PALMITATE
- POLYSORBATE 60
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
- HYALURONIC ACID
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)
- CETEARYL OLIVATE
- MENTHOL
- WATER
- HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS)
- CAPRYLYL GLYCOL
- SORBITAN ISOSTEARATE
- SODIUM CHLORIDE
- SORBITAN OLIVATE
- APRICOT KERNEL OIL
- SODIUM BENZOATE
- OATMEAL
- HYDROXYACETOPHENONE
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE)
- ALOE VERA LEAF
- 1,2-HEXANEDIOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53997-002 | 53997-002-01, 53997-002-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 29e5abb1-50cf-6438-e063-6294a90a1ae6 | 19357c7f-b7fa-dacc-e063-6394a90ad1c1 | 2024-12-22 | Warnings | 29e5abb1-50cf-6438-e063-6294a90a1ae6 19357c7f-b7fa-dacc-e063-6394a90ad1c1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


