Dch Scar Gel, Allantoin 0.5%

Dch Scar Gel, Allantoin 0.5%
SPL v2
SPL
SPL Set ID 00edbc64-9d32-5751-e063-6294a90a400b
Route
TOPICAL
Published
Effective Date 2021-07-20
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Allantoin (0.5 g)
Inactive Ingredients
Polyethylene Glycol 200 Tocopherol Panthenol Water Glycerin Onion Propylene Glycol Xanthan Gum Aloe Vera Leaf Black Walnut Chamomile Cucumber Alcohol Ethylhexylglycerin Benzyl Alcohol Hyaluronate Sodium

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2021-10-05
Description

Allantoin 0.5%

Medication Information

Warnings and Precautions

For external use only.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

Do not use on deep or puncture wounds, animal bites, and serious burns.

Indications and Usage

Apply as needed.

Dosage and Administration

Temporarily protects and helps relieve chapped or cracked skin.

Description

Allantoin 0.5%

Section 50565-1

Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away.

Section 51727-6

Water, Alcohol Denat., PEG-4, Propylene Glycol, Xanthan Gum, Allium Cepa (Onion) Bulk Extract, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Tocopherol, Glycerin, Juglans Nigra (Black Walnut) Leaf Extract, Ethylhexylglycerin, Benzyl Alcohol, Fragrance.

Section 51945-4

Section 55105-1

Skin Protectant.

Section 55106-9

Allantoin 0.5%

Structured Label Content

Indications and Usage (34067-9)

Apply as needed.

Dosage and Administration (34068-7)

Temporarily protects and helps relieve chapped or cracked skin.

Warnings and Precautions (34071-1)

For external use only.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days.

Do not use on deep or puncture wounds, animal bites, and serious burns.

Section 50565-1 (50565-1)

Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away.

Section 51727-6 (51727-6)

Water, Alcohol Denat., PEG-4, Propylene Glycol, Xanthan Gum, Allium Cepa (Onion) Bulk Extract, Panthenol, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Tocopherol, Glycerin, Juglans Nigra (Black Walnut) Leaf Extract, Ethylhexylglycerin, Benzyl Alcohol, Fragrance.

Section 51945-4 (51945-4)

Section 55105-1 (55105-1)

Skin Protectant.

Section 55106-9 (55106-9)

Allantoin 0.5%

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T12:04:55.789659 · Updated: 2026-03-14T23:06:06.305155