Drug profile

The FDA adverse-event record for Skin Conditioner (Unknown)

14 adverse-event reports submitted to the FDA Center for Veterinary Medicine reference Skin Conditioner (Unknown). See the species affected, top reactions, and outcomes below.

14
adverse-event reports
21.4%
death-coded share
Dog
most-reported species
5
Diarrhoea - top reaction
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Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
14
Total Reports
3
Deaths Reported
21.4%
Death Rate

Active Ingredients

Skin Conditioner (Unknown)

Administration Routes

TopicalUnknown

Species Affected

Dog 13
Goat 1

Most Affected Breeds

Terrier - Bull - Miniature 3
Retriever - Golden 2
Shih Tzu 2
Mastiff - Tibetan 2
Maltese 1
Pointing Dog - German Short-haired 1
Dog (unknown) 1
Boer or Boerbok 1
Terrier - Bull 1

Most Reported Reactions

Diarrhoea 5
Elevated gamma-glutamyl transferase (GGT) 4
Tense abdomen 4
Lethargy (see also Central nervous system depression in Neurological) 4
Lung sound 4
Emesis 3
Monocytosis 3
Increased respiratory rate 3
Low platelet count 3
Hypochloraemia 3
Eye redness 3
Decreased haematocrit 3

Outcome Breakdown

Outcome Unknown
6 (42.9%)
Euthanized
3 (21.4%)
Recovered with Sequela
2 (14.3%)
Ongoing
2 (14.3%)
Recovered/Normal
1 (7.1%)

Skin Conditioner (Unknown) Adverse Event Insights

14 reports name Skin Conditioner (Unknown); 3 recorded a death outcome (21.4% of reported events, not a population-level mortality rate). Active ingredient: Skin Conditioner (Unknown). Administration routes: Topical, Unknown.

By species: Dog (13 reports), Goat (1 reports). By breed: Terrier - Bull - Miniature (3), Retriever - Golden (2), Shih Tzu (2).

Leading clinical signs: Diarrhoea (5), Elevated gamma-glutamyl transferase (GGT) (4), Tense abdomen (4), Lethargy (see also Central nervous system depression in Neurological) (4). Outcome, 14 coded reports: Outcome Unknown leads at 42.9%.

Read these counts as reporting volume, not risk: per our methodology, a widely-prescribed drug will rack up more raw FDA reports in a given year than a rarely-used one at an identical true rate, so we recommend comparing within similar-exposure products rather than across the full 2025 catalog.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.