Winter Vanilla Hand Sanitizer

Winter Vanilla Hand Sanitizer
SPL v1
SPL
SPL Set ID fcbd0464-9d53-40a8-922b-8dc473790642
Route
TOPICAL
Published
Effective Date 2013-05-22
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Alcohol (75 1)
Inactive Ingredients
Water Carbomer Copolymer Type A (allyl Pentaerythritol Crosslinked) Trolamine Propylene Glycol Gelatin .alpha.-tocopherol Acetate Aloe Vera Leaf Ultramarine Blue Fd&c Red No. 4 Fd&c Yellow No. 5 Fd&c Blue No. 1 D&c Red No. 33

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH NOT FINAL Active Since 2013-05-22
Description

Active ingredient         purpose Alcohol 75%              Antiseptic

Medication Information

Warnings and Precautions

Warnings

For external use only.

FLAMMABLE. Keep away from flame or high heat.

When using this product

Avoid contact with eyes. If contact occurs, flush eyes with water.

Avoid contact with broken skin

Indications and Usage

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Dosage and Administration

Directions

Wet hands thoroughly with product and allow to dry without wiping.

For children under 6, use only under adult supervision.

Not recommended for infants.

Description

Active ingredient         purpose Alcohol 75%              Antiseptic

Section 50565-1

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Section 51727-6

Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).

May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).

Section 51945-4

limited time only

bodycology hand sanitizer

1 Fl Oz. 30 mL

Section 55105-1

Uses For hand washing to decrease bacteria on the skin.

Section 55106-9

Active ingredient         purpose

Alcohol 75%              Antiseptic

Structured Label Content

Indications and Usage (34067-9)

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Dosage and Administration (34068-7)

Directions

Wet hands thoroughly with product and allow to dry without wiping.

For children under 6, use only under adult supervision.

Not recommended for infants.

Warnings and Precautions (34071-1)

Warnings

For external use only.

FLAMMABLE. Keep away from flame or high heat.

When using this product

Avoid contact with eyes. If contact occurs, flush eyes with water.

Avoid contact with broken skin

Section 50565-1 (50565-1)

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Section 51727-6 (51727-6)

Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).

May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).

Section 51945-4 (51945-4)

limited time only

bodycology hand sanitizer

1 Fl Oz. 30 mL

Section 55105-1 (55105-1)

Uses For hand washing to decrease bacteria on the skin.

Section 55106-9 (55106-9)

Active ingredient         purpose

Alcohol 75%              Antiseptic

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

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Source: dailymed · Ingested: 2026-02-15T11:55:37.879453 · Updated: 2026-03-14T22:53:29.712463