Frida mom Perineal Healing Foam

Frida Mom by

Drug Labeling and Warnings

Frida Mom by is a Otc medication manufactured, distributed, or labeled by Prime Enterprises, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FRIDA MOM HEALING FOAM- salicylic acid aerosol, foam 
Prime Enterprises, Inc.

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Frida mom Perineal Healing Foam

Active ingredients

Witch Hazel 50%

Purpose

Astringent

Uses

• Helps relieve the local itching and discomfort in the perianal area.

Warnings

For external use only

When using this product

• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
• Do not exceed the recommended daily dosage unless directed by a doctor.
• Do not put this product into the rectum by using fingers or any mechanical device or applicator.

Stop use and ask a doctor if

• Rectal bleeding occurs.
• Condition worsens or does not improve within 7 days.

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

Directions

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Add foam on top of pad or pad liner. Children under 12 years of age: consult a doctor. Apply to the affected area up to 6 times daily or after each bowel movement.

Other information

• Store at room temperature

Inactive ingredients

Hamamelis Virginiana (Witch Hazel) Extract, Water, Glycerin, Alcohol, Sodium Lauroamphoacetate, Phenoxyethanol, Benzoic Acid, Tocopherol, Sodium Benzoate, Dehydroacetic Acid, Caprylic/Capric Triglyceride, Sodium Citrate, Mentha Piperita (Peppermint) Oil, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid

Frida mom Perineal Healing Foam

FRIDA MOM  HEALING FOAM
salicylic acid aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58443-0550
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WITCH HAZEL (UNII: 101I4J0U34) (WITCH HAZEL - UNII:101I4J0U34)	WITCH HAZEL	510 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
PEPPERMINT OIL (UNII: AV092KU4JH)
CHAMOMILE (UNII: FGL3685T2X)
SODIUM BENZOATE (UNII: OJ245FE5EU)
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZOIC ACID (UNII: 8SKN0B0MIM)
TOCOPHEROL (UNII: R0ZB2556P8)

Product Characteristics
Color	yellow (Very Light Yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58443-0550-4	139 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/21/2022	08/13/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	04/21/2022	08/13/2024

Labeler - Prime Enterprises, Inc. (101946028)

Registrant - Prime Enterprises, Inc. (101946028)

Establishment
Name	Address	ID/FEI	Business Operations
Prime Enterprises, Inc.		101946028	manufacture(58443-0550) , pack(58443-0550) , analysis(58443-0550) , label(58443-0550)

Revised: 8/2024

Document Id: 1f929914-7740-d78f-e063-6394a90aa862

34390-5

Set id: dd2dbffe-d839-16bc-e053-2995a90a7777

Version: 2

Effective Time: 20240813