DERMATECT MAX- emollient blend solution

DermaTect Max by

Drug Labeling and Warnings

DermaTect Max by is a Animal medication manufactured, distributed, or labeled by ProActive Solutions USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DermaTect Max

Hazard statement(s):
Not classified
Precautionary statement(s):
No labeling applicable
Hazards not otherwise classified: None under normal conditions
Storage and Disposal: Keep in a cool, well-ventilated place away from heat. Dispose of contents/container in accordance with licensed collector’s sorting instructions. Disposal must be done according to official regulations. Do not re-use empty containers.

First Aid:
General: If you feel unwell, seek medical advice.
Skin Contact: Wash skin with plenty of water.
Eye Contact: Rinse eyes with water as a precaution.
Ingestion: Call a poison center/doctor/physician if you feel unwell
Inhalation: Remove person to fresh air and keep comfortable for breathing.
Self protection of the first-aider: First aid workers
will be equipped with suitable personal protective
equipment.
Other medical advise or treatment: Treat
symptomatically.

DermaTect MaxTM is a versatile, 95% concentrated, triple emollient skin conditioning package designed for use with all ProActive Solutions’ concentrated teat dips to enhance skin condition performance in challenging environments.

MIXING INSTRUCTIONS:
Consult your local ProActive Solutions USA, LLC™ Quality Specialist.

DermaTect Max

INGREDIENTS AND APPEARANCE

DERMATECT MAX 
emollient blend solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 63927-4143
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	60.43 kg  in 100 kg
SORBITOL (UNII: 506T60A25R) (SORBITOL - UNII:506T60A25R)	SORBITOL	11.24 kg  in 100 kg
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	23.34 kg  in 100 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63927-4143-1	4.56 kg in 1 JUG
2	NDC: 63927-4143-2	22.8 kg in 1 DRUM
3	NDC: 63927-4143-3	68.4 kg in 1 DRUM
4	NDC: 63927-4143-4	250.72 kg in 1 DRUM
5	NDC: 63927-4143-5	1253.6 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
6	NDC: 63927-4143-6	1504.3 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/24/2025

Labeler - ProActive Solutions USA LLC (029368225)

Registrant - ProActive Solutions USA LLC (029368225)

Establishment
Name	Address	ID/FEI	Business Operations
ProActive Solutions USA LLC		029368225	api manufacture, manufacture, label, pack, repack

Establishment
Name	Address	ID/FEI	Business Operations
ProActive Solutions USA LLC		043147537	api manufacture, manufacture, label, pack, repack