Anal Care GLO pack
Active substance: SODIUM SULFATE, HYALURONATE SODIUM, PANTHENOL, ACTIVATED CHARCOAL, PEPPERMINT OIL, BORNEOL, GLYCERIN
CREAM · SODIUM SULFATE 1.33 g/100g, HYALURONATE SODIUM .017 g/100g, PANTHENOL .067 g/100g, ACTIVATED CHARCOAL .37 g/100g, PEPPERMINT OIL .1 g/100g, BORNEOL 2 g/100g, GLYCERIN 6.33 g/100g
United StatesActive
Marketing holder: WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM SULFATE · 1.33 g/100g
- HYALURONATE SODIUM · .017 g/100g
- PANTHENOL · .067 g/100g
- ACTIVATED CHARCOAL · .37 g/100g
- PEPPERMINT OIL · .1 g/100g
- BORNEOL · 2 g/100g
- GLYCERIN · 6.33 g/100g
Registration
- Registration number
- 84533-004
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- RECTAL, TOPICAL
Sources
- product · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 84533-004 · Verified 2026-10-09 · open in source