Neutraphorus Rex
FDA Label NDC 50952-003

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ph R&d Llc for the product Neutraphorus Rex (NDC 50952-003). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding other, active ingredient, purpose, uses, warnings, otc - when using, otc - stop use, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Other

→ Active Ingredient

→ Purpose

→ Uses

→ Warnings

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Do Not Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Questions?

→ Principal Display Panel - 57 G Jar

Other

Drug Facts

Active Ingredient

Dimethicone 1%

Purpose

Skin protectant

Uses

temporarily protects and helps relieve chapped or cracked skin
temporarily protects minor
cuts
scrapes
burns

Warnings

For external use only

Otc - When Using

When Using This Product

Keep out of eyes. Rinse eyes thoroughly with water to remove.

Otc - Stop Use

Stop Use And Ask A Doctor If

condition worsens
symptoms last more than 7 days or clear up and occur again within a few days

Otc - Do Not Use

Do Not Use On

deep or puncture wounds
animal bites
serious burns

Otc - Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

Apply cream liberally as often as needed

Inactive Ingredients

Water, Mineral Oil, White Petrolatum, Ceresin, Sorbitan Sesquioleate, Sorbitol, Lanolin Alcohol, Aluminum Hydroxide, Magnesium Hydroxide, BHT, Ethylhexylglycerin, Phenoxyethanol